WO2009086205A2

WO2009086205A2 - Body lumen filter

Info

Publication number: WO2009086205A2
Application number: PCT/US2008/087839
Authority: WO
Inventors: David Mackiewicz
Original assignee: Abbott Laboratories
Priority date: 2007-12-21
Filing date: 2008-12-19
Publication date: 2009-07-09
Also published as: WO2009086205A3

Abstract

The present invention concerns a luminal filter (10). The filter is formed to include: a plurality of filter elements (14) interconnected to form a filter body (12) shaped in a free recovery form and having a plurality of apertures (15) disposed between and defined by the interconnected filter elements. The apertures are dimensioned to inhibit particulates of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures. The filter body can include a first funnel (44) and second funnel (56) at least indirectly coupled together at their small ends. A polymeric wall contact (78a, b, 82a, b) can be coupled to the filter and disposed on an external surface thereof. A fastener (80a, b) can be used to secure the wall contact to the filter.

Description

BODY LUMEN FILTER

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of and priority to U.S. Provisional Patent Application No. 61/016,266 filed December 21, 2007 and entitled "Vena Cava Filter Having Wall Contacts"; claims the benefit of and priority to U.S. Provisional Patent Application No. 61/016,273 filed December 21, 2007, and entitled "Vena Cava Filter Having Hourglass Shape"; claims the benefit of and priority to U.S. Patent Application No. 12/338,980 filed December 18, 2008, and entitled "Vena Cava Filter Having Wall Contacts" which claims the benefit of and priority to U.S. Provisional Patent Application No. 61/016,266 filed December 21, 2007 and entitled "Vena Cava Filter Having Wall Contacts" and U.S. Provisional Patent Application No. 61/016,273 filed December 21, 2007, and entitled "Vena Cava Filter Having Hourglass Shape"; and claims the benefit of and priority to U.S. Patent Application No. 12/338,981 filed December 18, 2008, and entitled "Vena Cava Filter Having Hourglass Shape" which claims the benefit of and priority to U.S. Provisional Patent Application No. 61/016,266 filed December 21, 2007 and entitled "Vena Cava Filter Having Wall Contacts" and U.S. Provisional Patent Application No. 61/016,273 filed December 21, 2007, and entitled "Vena Cava Filter Having Hourglass Shape", each of which is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

1. The Field of the Invention

The present invention relates to a filter for use in a body lumen, such as the vena cava. More particularly, the present invention relates to a lumen filter that substantially has an hourglass shape or other substantially symmetrical shape about a central point.

2. Background

Vein thrombosis is a medical condition wherein a blood clot, or thrombus, has formed inside a vein. Such a clot often develops in the calves, legs, or lower abdomen, but can also affect other veins in the body. The clot may partially or completely block blood flow, and may break off and travel through the bloodstream as an embolus.

Commonly, the clot is caused by a pooling of blood in the vein, often when an individual is bed-ridden for an abnormally long duration of time, for example, when resting following surgery or suffering from a debilitating illness, such as a heart attack or traumatic injury. However, there are many other situations that cause the formation of a blood clot. Vein thrombosis is a serious problem because of the danger that the clot may break off and travel through the bloodstream to the lungs, causing a pulmonary embolism; a blockage of the blood supply to the lungs that causes severe hypoxia and cardiac failure and which frequently results in death. For many patients, anti-coagulant drug therapies may be sufficient to dissipate the clots. For example, patients may be treated with anticoagulants such as heparin and with thrombolytic agents such as streptokinase.

Unfortunately, some patients may not respond to or tolerate such drug therapies. Also, there may be other reasons why an anticoagulant is not desirable. For example, patients may have an acute sensitivity to heparin or may suffer from prolonged internal and/or external bleeding as a result of such drug therapies. Also, such drug therapies simply may be ineffective in preventing recurrent pulmonary emboli. In such circumstances, surgical procedures are typically required to prevent pulmonary emboli. Methods for prevention of primary or recurrent pulmonary emboli when anticoagulation therapies are ineffective are well-defined in the prior art. The current standard of therapy for prevention of pulmonary emboli in patients who are classified high-risk or who are unable to be anticoagulated is percutaneous insertion and placement of an inferior vena cava filter device.

Many presently used vena cava filters are permanently implanted in the inferior vena cava and remain for the duration of the patient's life or are removably implanted, but which still remain in position for long durations. As such, the filters can incur tissue ingrowth from the surrounding tissue, often resulting in a decreased blood flow and/or in blood clots. While some permanent filters are designed to be percutaneously retrievable, they often become embedded as their anchoring features become endothelialized by the vessel wall and retrieval must be done surgically.

BRIEF SUMMARY OF THE INVENTION

The present invention provides a filter for use in a body lumen. For example, filter may be a vena cava filter. More particularly, the present invention provides a lumen filter that substantially has an hourglass shape or other substantially symmetrical shape about a central point that may be formed by being laser cut from a tube or braided and then formed into the free recovery shape to longitudinally elongate and radially collapse during deployment or retrieval and to longitudinally shorten and radially expand after being set. The vena cava filter may also have wall contacts (e.g., biodegradable polymer) that separate the filter from the inner surface of the body lumen to inhibit endothelial cell ingrowth into the lumen filter.

In one embodiment, the present invention provides a filter having a wall contact for use in a body lumen of a subject. Such a filter includes: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, the apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures, and at least one biodegradable wall contact coupled to at least one of the filter elements on the external surface of the filter body, the wall contact having an initial thickness dimension that is substantially orthogonal to central axis of the filter body and that separates the external surface from an inner wall of the body lumen.

In one embodiment, the present invention provides a filter having a removable wall contact for use in a body lumen of a subject. Such a filter includes: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, the apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures, at least one filter element defining at least one fastener hole extending from the external surface to the internal surface, at least one fastener extending through the at least one fastener hole, and at least one biodegradable wall contact removably coupled to the at least one filter element on the external surface of the filter body by being coupled to the at least one fastener extending through the at least one fastener hole, the wall contact having an initial thickness dimension that is substantially orthogonal to central axis of the filter body and that separates the external surface from an inner wall of the body lumen.

In one embodiment, the filter body has at least one of the following: a substantially funnel shape with a conduit having a larger end opposite of a smaller end, said smaller end being dimensioned to inhibit a thrombus of a selected size from passing therethrough, a substantially cone shape with a cavity having a larger end opposite of an apex to inhibit a thrombus of a selected size from passing therethrough, or a substantially hourglass shape with a conduit having a narrow median portion being dimensioned to inhibit a thrombus of a selected size from passing therethrough. In one embodiment, the wall contact further includes at least one of the following: a square to rectangular block cross section, a square to rectangular block cross section having a long dimension that extends from the external surface of the filter body, a square to rectangular block cross section having a concave surface coupled to the external surface of the filter body, a square to rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen, an opposite convex surface configured to conform with the inner wall of the body lumen, or an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen.

In one embodiment, at least one wall contact has a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject. As such, the longitudinal length of the wall contact has a dimension from about 0 (or 0.0001 millimeters) to about 10 millimeters, or any size therebetween.

In one embodiment, the wall contact is dimensioned to inhibit endothelial cell ingrowth into the apertures.

In one embodiment, the filter includes at least one of the following: the wall contact being coated onto the external surface to extend into at least a portion of the plurality of apertures, a filter element defining a hole with a portion of the wall contact extending therethrough, a filter element defining a hole with a fastener extending therethrough and coupling with the at least one wall contact, a filter element defining a hole shaped as a keyway slot and a portion of the wall contact extending therethrough, a filter element defining a hole shaped as a keyway slot with a fastener extending therethrough and coupling with the at least one wall contact, a filter element defining a hole shaped as a keyway slot having a large portion and a narrow portion and a portion of the wall contact extending therethrough, the portion of the wall contact having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot, or a filter element defining a hole shaped as a keyway slot having a large portion and a narrow portion with a fastener extending therethrough and coupling with the at least one wall contact, the fastener having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

In one embodiment, the wall contact is formed from a biodegradable polymer selected from the group consisting of a natural polymer, synthetic polymer, polysaccharide, starch, cellulose, protein, gelatin, casein, polyesters, polyhydroxyalkanoates, lignin, shellac, natural rubber, polyalkylene esters, polylactic acids, polylactides, polyglycolic acids, polyglycolides, polyamide esters, polyvinyl esters, polyvinyl alcohols, polyanhydrides, polyesters, salts thereof, copolymers thereof, and combinations thereof.

In one embodiment, the present invention provides a method of manufacturing a filter having a wall contact for use in a body lumen of a subject. Such a method includes: forming a filter body including a plurality of filter elements interconnected together such that the filter body has a plurality of apertures disposed between and defined by the interconnected filter elements, the apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures; forming at least one fastener hole in the filter body to extend from the external surface to the internal surface, inserting at least one fastener extending through the at least one fastener hole, and coupling at least one biodegradable wall contact to the external surface of the filter body by being coupled to the at least one fastener extending through the at least one fastener hole, the wall contact having an initial thickness dimension that is substantially orthogonal to central axis of the filter body and that separates the external surface from an inner wall of the body lumen.

In one embodiment, the method of manufacture includes at least one of the following: forming the wall contact to have a square to rectangular block cross section, forming the wall contact to have a square to rectangular block cross section having a long dimension that extends from the external surface of the filter body, forming the wall contact to have a square to rectangular block cross section having a convex surface coupled to the external surface of the filter body, forming the wall contact to have a square to rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen, forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen, or forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen.

In one embodiment, the method of manufacture further includes forming the wall contact to have a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject.

In one embodiment, the method of manufacture further includes: forming the at least one fastener hole shaped as a keyway slot having a large portion and a narrow portion and forming the at least one fastener to have a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

In one embodiment, the present invention is a filter for use in a body lumen of a subject. Such a filter includes a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements. The apertures are dimensioned to inhibit a thrombus of a selected size from passing through the apertures and are dimensioned to allow blood components smaller than the selected size to pass through the apertures. The filter body includes: a first funnel having a first funnel-shaped body defining a first conduit having a first larger end fluidly coupled to and opposite of a first smaller end, the first funnel-shaped body having a plurality of first apertures defined by the interconnected filter elements and a second funnel having a second funnel-shaped body defining a second conduit having a second larger end fluidly coupled to and opposite of a second smaller end, the second funnel-shaped body having a plurality of second apertures defined by the interconnected filter elements, the second smaller end of the second funnel is fluidly coupled to the first smaller end of the first funnel, the first smaller end and second smaller end are dimensioned to inhibit a thrombus of a selected size from passing therethrough.

In one embodiment, a luminal filter includes the following: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, the apertures are dimensioned to inhibit a thrombus of a selected size from passing through the apertures and are dimensioned to allow blood components smaller than the selected size to pass through the apertures, a first funnel having a first funnel-shaped body defining a first conduit having a first larger end fluidly coupled to and opposite of a first smaller end, the first funnel- shaped body having a plurality of first apertures defined by the interconnected filter elements, a second funnel having a second funnel-shaped body defining a second conduit having a second larger end fluidly coupled to and opposite of a second smaller end, the second funnel-shaped body having a plurality of second apertures defined by the interconnected filter elements, and a median portion having a median body defining a median conduit having a first end coupled to the first smaller end of the first funnel and having a second end coupled to the second smaller end of the second funnel, the median conduit being dimensioned to inhibit a thrombus of a selected size from passing through the median conduit.

In one embodiment, the filter body is configured such that the first larger end of the first funnel and the second larger end of the second funnel each have a reduced dimension when tensile longitudinal forces are applied to the filter body. Also, the filter body is configured such that the first larger end of the first funnel and the second larger end of the second funnel each have an enlarged dimension when compressive longitudinal forces are applied to the filter body. In one embodiment, the filter body further includes at least one of the following: a first tube having a first tube-shaped body defining a first tube conduit and having a first end fluidly coupled to the first larger end of the first funnel-shaped body, said first tube having a first length, or a second tube having a second tube-shaped body defining a second tube conduit and having a second end fluidly coupled to the second larger end of the second funnel-shaped body, said second tube having a second length. The first length of the first tube and/or the second length of the second tube can be dimensioned to inhibit the filter from migrating within the body lumen of the subject. This can include at least one of the first length or second length having a dimension from about 0 (or 0.0001 millimeters) to about 10 millimeters, or any size therebetween. In one embodiment, at least one of the first funnel or second funnel is shaped to trap the thrombus of the selected size within the respective conduit at a central axial position and to allow removal of the thrombus when the filter is removed. At least one of the first apertures or second apertures are dimensioned to inhibit the thrombus of the selected size from passing therethrough and being dimensioned to allow blood components smaller than the selected size to pass therethrough.

In one embodiment, the filter body has sufficient rigidity to reconfigure the body lumen from an oblong-shaped cross section to a circular- shaped cross section. In one embodiment, the interconnected filter elements are formed from laser shaping the filter body. In one embodiment, the interconnected filter elements are formed from braids.

In one embodiment, the present invention provides a method of utilizing a luminal filter in a body lumen of a subject. Such a method includes the following: providing a luminal filter having a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, the apertures being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures, the filter body is configured as described herein, longitudinally elongating the filter body such that the larger ends of the filter have a reduced dimension, delivering the elongated filter body to a desired deployment site within the body lumen of the subject, and longitudinally shortening the filter body such that the larger ends of the filter each have an enlarged dimension that applies radial forces to an inner wall of the body lumen.

In one embodiment, such a method can optionally further include: longitudinally elongating the filter body such that the larger ends filter have a reduced dimension with a cross section that is smaller than the body lumen and retrieving the elongated filter body from the desired deployment site within the body lumen of the subject.

In one embodiment, at least one of delivering or retrieving the filter is performed with a catheter. These and other embodiments and features of the present invention will become more fully apparent from the following description and appended claims, or may be learned by the practice of the invention as set forth hereinafter.

BRIEF DESCRIPTION OF THE DRAWINGS To further clarify the above and other advantages and features of the present invention, a more particular description of the invention will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. It is appreciated that these drawings depict only typical embodiments of the invention and are therefore not to be considered limiting of its scope. The invention will be described and explained with additional specificity and detail through the use of the accompanying drawings. Moreover, the features of the drawings are not drawn to scale it is understood that one of ordinary skill in the arts would understand the appropriate size and size- relatedness of the various features shown in the figures. Figure IA is a schematic representation illustrating a side view of an embodiment of a filter having wall contacts.

Figure IB is a cross-sectional view of the filter of Figure IA.

Figures 2A-2D are schematic representations illustrating side views of embodiments of filters having wall contacts. Figures 3A-3F are schematic representations illustrating cross-sectional profiles for embodiments of filters having wall contacts.

Figure 4A is a schematic representation illustrating a side view of an embodiment of a conical filter having wall contacts coupled to the filter via a fastener inserted through fastener holes. Figure 4B is a magnified cutaway side view of Figure 4A illustrating an embodiment of the fastener inserted through fastener holes in order to couple the wall contact to the filter.

Figure 4C is a magnified cutaway view of Figure 4B illustrating an embodiment of the fastener holes having a keyway slot shape. Figure 5A is a schematic representation illustrating a cutaway view of an embodiment of a delivery system delivering an embodiment of the filter into a body lumen.

Figure 5B is a schematic representation illustrating a cutaway view of the filter of Figure 5A after being deployed within the body lumen. Figure 6A is a schematic representation illustrating a side view of an embodiment of a filter having a free recovery shape.

Figure 6B is a cross-sectional view of the filter of Figure 6A.

Figures 7A-7D are schematic representations illustrating side views of embodiments of filters having free recovery shapes. Figures 8A-8F are schematic representations illustrating cross-sectional profiles for embodiments of filters having a free recovery shape.

Figure 9A is a schematic representation illustrating a cutaway view of an embodiment of a delivery system delivering an embodiment of the filter into a body lumen. Figure 9B is a schematic representation illustrating a cutaway view of the filter of Figure 9A after being deployed within the body lumen.

DETAILED DESCRIPTION The present invention provides a filter for use in a body lumen, such a lumen filter can be configured as a vena cava filter. More particularly, the present invention provides a lumen filter that optionally has wall contacts (e.g., biodegradable polymer) that separate the filter from the inner surface of the body lumen to inhibit endothelial cell ingrowth into the lumen filter. The lumen filter can also have a substantially hourglass shape or other substantially symmetrical shape about a central point that may be formed by being laser cut from a tube or braided and then formed into the free recovery shape to longitudinally elongate and radially collapse during delivery and/or retrieval and to longitudinally shorten and radially expand after being set. Optionally, the filter is substantially half of the hourglass shape to be conical or funnel shaped. The substantially hourglass shape, conical shape, and/or funnel shape can be referred to as a free recovery shape because it allows for the body to longitudinally elongate and radially collapse during delivery or retrieval and to longitudinally shorten and radially expand after being set. Thus, the free recovery shape may facilitate delivery and may provide for the possibility of retrieval. I. Introduction Accordingly, the present invention is a filter that is implantable in a blood vessel or other lumen in the body of the patient. Such filters may utilize one or more members arranged to capture particulates within the blood flow, without substantially interfering with the normal blood flow. Such a filter can be formed from a shape memory material for implantation into a vessel and subsequent extraction therefrom. The filter may have wall contacts (e.g., biodegradable polymer) that separate the filter from the inner surface of the body lumen. The vascular filter may capture particulates (e.g. thrombus) within the blood flow in the vessel and may retain such particulates during extraction. Prior to implantation, the filter is generally longitudinally elongated and radially collapsed. The filter can be delivered with a delivery device that is compatible with or includes a catheter. After being inserted to the place of deployment, the filter reverts to a predetermined shape that is suitable for filtering the blood flow by radially expanding and longitudinally shortening.

The predetermined shape of the filter may include a plurality of interconnected members that are disposed about a longitudinal axis and that may form a bi-conical shape, symmetric cylindrical shape, funnel shape, or hourglass shape portions in order to provide the free recovery shape. The bi-conical or hourglass shape can be described as two funnels or funnels coupled at or near their respective tips or a portion of each funnel or funnel proximal of a tip or central axis, which can include the bottom aperture of two conical members being joined so that a conduit of appropriate size may extend therethrough. When referred to as funnels, the filter includes two funnels coupled together at or near their small openings.

In an embodiment, the filter of the present invention is a vena cava filter. The vena cava filter can be implantable in the inferior vena cava and may be utilized to filter peripheral venous blood clots, a thrombus, and/or other appropriately sized particulates. The filter can be permanently or removably implanted, which may be facilitated by the wall contacts that separate the filter from the inner surface of the body lumen. While the free recovery design may allow for a more readily extractable filter, the filter may also be suitable for long-term or permanent implantation. Accordingly, the filter can be configured to be deployed at the aortic arch of the aorta providing cerebral embolic protection. The filter can be positioned in the base of the aortic arch, between the aortic valve and the brachiocephalic artery. Any potential emboli may be captured by the filter, thereby inhibiting entry into the neurovasculature. However, the filter of the present invention can be positioned at any suitable portion of the vena cava, or even configured for deployment in a non- vasculature lumen such as the urethra.

In one embodiment, multiple filters of the present invention can be employed. For example, a first filter can be positioned in the brachiocephalic artery and a second filter can be positioned in the left common carotid artery of the aortic arch. Any potential emboli may thereby be captured by the filters to inhibit entry into the neurovasculature. In a further embodiment, the filter of the present invention may be utilized as anatomic junction or bridge. An anatomic junction can be used in the repair of damaged or grafted vessels. Also, the filter can be used similarly as a stent.

In one embodiment, the present invention is a filter for use in a body lumen of a subject. Such a filter may include a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and may be defined by the interconnected filter elements. The apertures may be dimensioned to inhibit a thrombus of a selected size from passing through the apertures and may be dimensioned to allow blood components smaller than the selected size to pass through the apertures. At least one wall contact (e.g., biodegradable polymer) may be disposed on the filter body to separate the filter from the inner surface of the body lumen and/or to anchor the filter in place. In one embodiment, the filter body may include a first funnel having a first funnel- shaped body defining a first conduit having a first larger end fluidly coupled to and/or opposite of a first smaller end. The first funnel-shaped body has a plurality of first apertures defined by the interconnected filter elements.

In one embodiment, the filter body may include a second funnel having a second funnel-shaped body defining a second conduit having a second larger end fluidly coupled to and/or opposite of a second smaller end. The second funnel-shaped body has a plurality of second apertures defined by the interconnected filter elements. The second smaller end of the second funnel is fluidly coupled to the first smaller end of the first funnel, the first smaller end and second smaller end are dimensioned to inhibit a thrombus of a selected size from passing therethrough.

In one embodiment, the luminal filter may include a median portion having a median body defining a median conduit having a first end coupled to the first smaller end of the first funnel and having a second end coupled to the second smaller end of the second funnel. The median conduit may be dimensioned to inhibit a thrombus of a selected size from passing through the median conduit.

In one embodiment, the lumen filter body is configured such that the first larger end of the first funnel and/or the second larger end of the second funnel each have a reduced dimension when tensile longitudinal forces are applied to the filter body. Also, the filter body may be configured such that the first larger end of the first funnel and/or the second larger end of the second funnel each have an enlarged dimension when compressive longitudinal forces are applied to the filter body.

In one embodiment, the filter body further includes at least one of the following: a first tube having a first tube-shaped body defining a first tube conduit and having a first end fluidly coupled to the first larger end of the first funnel-shaped body, said first tube having a first length or a second tube having a second tube- shaped body defining a second tube conduit and having a second end fluidly coupled to the second larger end of the second funnel-shaped body, said second tube having a second length. The first length of the first tube and/or the second length of the second tube can be dimensioned to inhibit the filter from migrating within the body lumen of the subject. This can include at least one of the first length or second length having a dimension from about 0 millimeters (or 0.0001 mm) to about 10 millimeters, or any size therebetween. In one embodiment, the first funnel is shaped to trap the thrombus of the selected size within the respective conduit at a central axial position and/or to allow removal of the thrombus when the filter is removed. The filter body may have sufficient rigidity to reconfigure the body lumen from an oblong-shaped cross section to a circular- shaped cross section. The interconnected filter elements may be formed from laser shaping the filter body. The interconnected filter elements may be formed from braids.

In one embodiment, the present invention provides a method of utilizing a luminal filter in a body lumen of a subject. Such a method includes the following: providing a luminal filter as described herein, longitudinally elongating the filter body such that the large ends of the filter have a reduced dimension, delivering the elongated filter body to a desired deployment site within the body lumen of the subject, and longitudinally shortening the filter body such that the large ends of the filter each have an enlarged dimension that applies radial forces to an inner wall of the body lumen through the wall contacts. In one embodiment, such a method can optionally further include: longitudinally elongating the filter body such that the larger ends filter have a reduced dimension with a cross section that is smaller than the body lumen and retrieving the elongated filter body from the desired deployment site within the body lumen of the subject.

In one embodiment, at least one of delivering or retrieving the filter is performed with a catheter.

II. Lumen Filter

Generally, the filter of the present invention includes a filter body disposed about a longitudinal axis. The filter can be made of a shape memory alloy, which when in a delivery and/or retrieval orientation has at least a first portion that is in a narrowed configuration, and when deployed and set having an expanded configuration. The filtering portion, which may be substantially conical, can be configured to be similarly narrowed during delivery and/or retrieval and expanded after being deployed and set. This provides the free recovery shape. However, the conical portion can be configured to maintain substantially a constant size during deployment and after being deployed and set. The largest diameter portion of the filter may have a diameter of sufficient size to contact the inner walls of the vessel. As such, the largest diameter portion of the filter can provide a force against the inner wall of the vessel to hold the filter at the site of deployment. The large diameter portion of the filter can also have a wall contact disposed on the external surface. The wall contact may be dimensioned sufficiently to separate the filter body from the inner surface of the body lumen. Accordingly, increasing the area of the wall contact can increase the contact area with the vessel and/or decrease the chance for the filter to move from the site of deployment. The force of the large diameter portion and/or wall contact applied to the inner surface of the vessel may act together to anchor and/or stabilize the filter at the site of deployment within the vessel.

The large diameter portion of the filter can also have a wall contact disposed on the external surface. The wall contact may be dimensioned sufficiently to separate the filter body from the inner surface of the body lumen. Accordingly, increasing the area of the wall contact can increase the contact area with the vessel and/or decrease the chance for the filter to move from the site of deployment. The force of the large diameter portion and/or wall contact applied to the inner surface of the vessel may act together to anchor and stabilize the filter at the site of deployment within the vessel. The narrowed section, which includes the conical portion, may be formed by strut elements and/or braids (e.g., filter elements) that may provide a conduit having a progressively decreasing diameter between the large end and the small end of each funnel. The strut elements and/or braids can be provided in a spaced apart arrangement of an appropriate distance to capture particulates within the blood flow without substantially interfering with the normal blood flow.

Generally, a filter of the present invention can include at least a first set of interconnected strut elements (e.g., filter elements) that cooperatively define the body of the filter. Usually, each strut element can be defined by a cross-sectional profile as having a width and a thickness, and including a first end and a second end bounding a length. The stent element can be substantially linear, arced, rounded, squared, combinations thereof, or other configurations. The strut element can include a bumper, crossbar, connector, inter-connector, intersection, elbow, foot, ankle, toe, heel, medial segment, lateral segment, combinations thereof, or the like. Generally, the strut element can be configured to a corresponding element of a stent. The wall contacts can be formed into various shapes and sizes, and a range in the number of wall contacts can be varied for different uses. Generally, the wall contact is polymeric and dimensioned sufficiently to separate the filter body from the vessel wall and/or anchor the filter in place. The present invention provides a filter having a free recovery shape that may allow for easy delivery and/or retrieval. Accordingly, the figures illustrate embodiments of filters that have the free recovery shapes. While the filters are shown to have symmetrical portions that are substantially hourglass in shape, the filters can be substantially half of an hourglass, conical, or funnel-like shape. As such, the embodiments of the filters of the present invention can be half of the shape that is shown in the figures.

Figure IA is a schematic representation of an embodiment of a filter 10 having a central axis 76, which is shown in side view, in accordance with the present invention. The filter 10 has an hourglass-like shape that is defined by the filter body 12, which includes a first body portion 20, second body portion 32, first funnel body 44, second funnel body 56, and median body 68. The filter 10 is arranged such that the first body portion 20 is coupled to the first funnel body 44, which is coupled to the median body 68 which is coupled to the second funnel body 56 which is coupled to the second body portion 32. The filter body 12 can include a plurality of structural elements 14 (e.g., strut elements, braids, or the like) that cooperate to provide structural integrity to the filter 10. The body 12 and body elements 14 can be shaped and/or otherwise configured similarly to an endoprosthesis configured for deployment into a body lumen, examples of which include lumen filters, stents, and the like. The structural elements 14 can include annular elements, helical elements, crossbars, connectors, junctions, braids, and other like features that may be employed in stent and/or filter endoprostheses.

The hourglass shape of the body 12 at least partially defines a first end 16 that includes a first opening 18 formed therein. The first end 16 is disposed at a longitudinal end of the body 12, and the first opening 18 can be substantially the same dimensions as the first end 16. The segment of the body 12 that defines the first end 16 is the first body portion 20. The first body portion 20 can have various shapes and sizes; however, it is depicted as being substantially cylindrical in Figure IA. The first body portion 20 defines a first large conduit 22 that is fluidly coupled with the first opening 18 such that an object can pass through the first opening 18 and into the first large conduit 22, or vice versa. The first large conduit 22 has a first large diameter 24 that has a uniform or varying dimension. The first large diameter 24 can be substantially uniform such that the first body portion 20 has a substantially uniform cross-sectional profile. The first body portion 20 and/or the first large conduit 22 has a first length 26 that extends from the first end 16 and/or first opening 18 to the opposite end of the first body portion 20 and/or first large conduit 22.

Additionally, the opposite end of the hourglass shape of the body 12 from the first end 16 at least partially defines a second end 28 that includes a second opening 30 formed therein. The second end 28 is disposed at a longitudinal end of the body 12, and the second opening 30 can be substantially the same dimensions as the second end 28. The segment of the body 12 that defines the second end 28 is the second body portion 32. The second body portion 32 can have various shapes and sizes; however, it is depicted as being substantially cylindrical in Figure IA, which is similar to the first body portion 20. The second body portion 32 defines a second large conduit 34 that is fluidly coupled with the second opening 30 such that an object can pass through the second opening 30 and into the second large conduit 34, or vice versa. The second large conduit 34 has a second large diameter 36 that has a uniform or varying dimension. The second large diameter 36 can be substantially uniform such that the second body portion 32 has a substantially uniform cross-sectional profile. The second body portion 32 and/or the second large conduit 34 has a second length 38 that extends from the second end 28 and/or second opening 30 to the opposite end of the second body portion 32 and/or second large conduit 34.

The first body portion 20 is fluidly coupled with a first funnel body 44 such that the end of the first body portion 20 opposite of the first end 16 and/or first opening 18 is coupled to the first funnel large end 40. As such, the first funnel large end 40 can be considered to be a junction with the first body portion 20. The first funnel body 44 also has a first funnel small end 42 that is opposite of the first funnel large end 40. As shown, the first funnel large end 40 has a larger diameter and/or opening compared to the first funnel small end 42. The first funnel body 44 defines a first funnel conduit 50 which is disposed therein. The first funnel body 44 and/or first funnel conduit 50 includes a first funnel diameter 46 that decreases from the first funnel large end 40 to the first funnel small end 42 such that the cross-sectional profile of the first funnel body 44 and/or first funnel conduit 50 correspondingly decreases. The first funnel body 44 and/or the first funnel conduit 50 has a first funnel length 48 that extends from the first funnel large end 40 to the opposite first funnel small end 42.

The second body portion 32 is fluidly coupled with a second funnel body 56 such that the end of the second body portion 32 opposite of the second end 28 and/or second opening 30 is coupled to the second funnel large end 52. As such, the second funnel large end 52 can be considered to be a junction with the second body portion 32. The second funnel body 56 also has a second funnel small end 54 that is opposite of the second funnel large end 52. As shown, the second funnel large end 52 has a larger diameter and/or opening compared to the second funnel small end 54. The second funnel body 56 defines a second funnel conduit 62 which is disposed therein. The second funnel body 56 and/or second funnel conduit 62 includes a second funnel diameter 58 that decreases from the second funnel large end 52 to the second funnel small end 54 such that the cross-sectional profile of the second funnel body 56 and/or second funnel conduit 62 correspondingly decreases. The second funnel body 56 and/or the second funnel conduit 62 has a second funnel length 60 that extends from the second funnel large end 52 to the opposite second funnel small end 54.

The first funnel small end 42 of the first funnel body 44 is coupled to the first median end 64 of the median body 68, and the second funnel small end 54 of the second funnel body 56 is coupled to the second median end 66 of the median body 68. This configuration disposes the median body 68 between the first funnel body 44 and the second funnel body 56. The median body 68 defines a median conduit 74, having a median diameter 70 and a median length 72. The median diameter 70 can have a dimension that is substantially the same from the first median end 64 to the second median end 66, or the dimension can be varied, such as increasing, decreasing, parabolic, and the like.

The filter 10 can be configured such that each corresponding portion along the central axis 76 is similar or different. For example, the first body portion 20 can have shapes and/or dimensions that are the same or different from the shapes and/or dimensions of the second body portion 32; the first funnel body 44 can have shapes and/or dimensions that are the same or different from the shapes and/or dimensions of the second funnel body 56. Also, the median body 68 can be configured such that the median conduit 74 is extremely small so that blood clot particulates do not pass therethrough. This allows the filter 10 to filter the blood. Also, the first length 26 of the first body portion 20 and/or the second length 38 of the second body portion 32 can be dimensioned to improve the static disposition of the filter 10 within a body lumen such that the filter 10 is substantially immobile after deployment. This can impart an enlarged contact surface with the body lumen that allows the filter 10 to have increased contact with the body lumen. Additionally, the first funnel length 48 and/or second funnel length 60 can be dimensioned to improve the filtering capability of the filter 10, wherein such dimension changes can include sharper or more gradual slopes of the conical shape. Moreover, the dimensions of the median body 68 can be modulated to change the filtering characteristics of the filter 10, where a smaller median conduit 74 can catch smaller particles and a larger median conduit 74 can allow larger particles to pass therethrough. Thus, the diameter, shape, and/or length of the median conduit 74 can be tailored for a particular body lumen and/or for the size of particulates to be captured and filtered from the body fluid.

Additionally, Figure IA illustrates the filter 10 having wall contacts 78a,b and 82a,b. The first wall contacts 78a,b are disposed on the filter body 12 on an exterior surface of the first body portion 20. As shown, the first body portion 20 includes a first wall contact 78a that is coupled to the filter body 12 by having fasteners 80a,b that are coupled to at least one of the structural elements 14. This can include the fasteners 80a,b extending through a hole (not shown) in a structural element 14 and coupling to the first wall contact 78a. The fasteners 80a,b can be any type of fastener element that can attach the first wall contact 78a with the first body portion 20 of the filter body 12. Additionally, a first opposite wall contact 78b is disposed on the external surface of the first body portion 20 of the filter body 12 opposite from the first wall contact 78a. The first opposite wall contact 78b is coupled to the first body portion 20 of the filter body 12 by fasteners 80c,d, which can be substantially similar to fasteners 80a,b. For example, the large diameters 24, 36 can be from about 0.001 mm to about 10 mm, from about 0.01 mm to about 5 mm, and/or about 0.1 mm to about 1 mm. The lengths 26, 38 can be from about 0 mm to about 50 mm, from about 0.001 to about 25 mm, and/or about 0.1 mm to about 10 mm. The funnel diameters 46, 58 can be from about 0 mm to about 10 mm, from about 0.001 mm to about 5 mm, and/or about 0.01 mm to about 1 mm. The funnel lengths 48, 60 can be from about 0.01 mm to about 50 mm, from about 0.1 mm to about 25 mm, and/or about 0.5 mm to about 1 mm. The median diameter 70 can be from about 0 mm to about 1 mm, from about 0.0001 mm to about 0.5 mm, and/or about 0.001 mm to about 0.01 mm. The median length 72 can be from about 0 mm to about 50 mm, from about 0.001 mm to about 25 mm, and/or about 0.01 mm to about 10 mm. However, other sizes and/or shapes can be employed and determined by routine studies of the vasculature or other body lumen in which the filter 10 will be placed.

The second wall contacts 82a, b are disposed on the filter body 12 on an exterior surface of the second body portion 32. As shown, the second body portion 32 includes a second wall contact 82a that is coupled to the filter body 12 by having fastener 84a coupled to at least one of the structural elements 14. This can include the fastener 84a extending through a hole (not shown) in a structural element 14 and coupling to the second wall contact 82a. The fastener 84a can be any type of fastener element that can attach the second wall contact 82a with the second body portion 32 of the filter body 12. Additionally, a second opposite wall contact 82b is disposed on the external surface of the second body portion 32 of the filter body 12 opposite from the second wall contact 82a. The second opposite wall contact 82b is coupled to the second body portion 32 of the filter body 12 by fastener 84b, which can be substantially similar to fastener 84a. The wall contacts 78, 82 are shown to have a length that is substantially similar to the body portion to which they are coupled. For example, first wall contacts 78a,b are shown to be substantially the same length as the first body portion 20, and the second wall contacts 82a,b are shown to be substantially the same length as the second body portion 32. However, any of the contacts can be any length with respect to the body portion to which they are coupled, which can be longer or shorter. Also, while one wall contact is shown to be disposed on a body portion in a given length, a plurality of wall contacts can be disposed on the body portion in a given length. For example, the first wall contact 78a can include a plurality of wall contacts that can be adjacently touching or separated along the first length 26 of the first body portion 20. Also, each of the first wall contacts 78a,b are shown to be coupled to the first body portion 20 via two fasteners 80 and each of the second wall contacts 82a,b are shown to be coupled to the second body portion 32 via one fastener 82; however, any number of fasteners can be used to couple a wall contact to the filter 10.

Figure IB is a schematic representation of a cross- sectional profile of the filter 10 taken at line IB show in Figure IA, which mainly depicts the cross-sectional profile of the first body portion 20, the first funnel body 44, and the median conduit 74. As shown, and with further reference to Figure IA, the first body portion 20 has a diameter 24 that is substantially similar to the size of the first funnel large end 40. The first funnel body 44 narrows the first funnel conduit 50 until reaching the small opening of the median conduit 74, which has a small median diameter 70. The first funnel body 44 can include a plurality of structural elements 14 that cooperate to form filter apertures 15 that are filter pores. The size and/or shapes of the filter apertures 15 can be configured to be larger or smaller depending on the size of particulates to be trapped and filtered from the body fluid. For example the apertures 15 can have a dimension ranging from about 0.00001 mm to about 0.1 mm, from about 0.0001 mm to about 0.01 mm, and/or from about 0.001 mm to about 0.001 mm.

Figure IB also shows the first wall contact 78a to be disposed oppositely of the first opposite wall contact 78b. Additionally, the first body portion 20 can include additional first wall contacts 78c,d disposed around the outer surface of the body 12. While four wall contacts 78a-d are shown to be disposed on the outer surface of the first body portion 20, any number of wall contacts 78a-d can be used. Also, the wall contacts 78a-d can be systematically, evenly, randomly, unevenly, or otherwise distributed around the circumference of the first body portion 20. Figures IA- IB also show an example of an embodiment of the configuration of the structural elements 14 and the corresponding filter apertures 15. As shown, the filter apertures 15 proximate to the first funnel large end 40 have substantially the same dimensions as the filter apertures 15 that are proximate to the first funnel small end 42. However, the filter apertures 15 proximate to the first funnel large end 40 can be larger than the filter apertures 15 that are proximate to the first funnel small end 42, or vice versa. However, the filter apertures 15 can have any functional shape and/or size to function as a filter pore.

Figures 2A-2D illustrate schematic representations of additional embodiments of an endoprosthesis in accordance with the present invention. As illustrated, the endoprosthesis can be configured into a filter for a body lumen.

Figure 2A is a schematic representation of a side view of a filter 200 in accordance with the present invention. The filter 200 has a shape and size that is defined by a filter body 202 having an interconnected diamond pattern. As shown, the filter body 202 is in the shape of a double cone filter. That is, the filter body 202 is shaped substantially similarly to two cones 204, 206 that are coupled together at the median point 208. The various features of the filter body 202 can be configured similarly to the filter 100 of Figure IA. Accordingly, the first cone 204 can have an opening that allows a body fluid to flow therethrough with the filter body 202 forming a first cone 204 that decreases the cross-sectional profile until reaching the median point 208. The second cone 206 may be substantially similar to the first cone 204; however, it may be oriented in the opposite direction. This may allow the filter 200 to be bi-directional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid. Figure 2A also shows first wall contacts 211a,b disposed on the first cone 204, which may be coupled thereto via fasteners 212a,b. Also, second wall contacts 214a,b are shown to be disposed on and coupled to the second cone 206 via fasteners 216a,b. The wall contacts 211,214 are shown to have an outer surface configured to conform to the wall of body lumen to provide a contact surface therewith, and to have an inner surface configured to conform to the sloped outer surface of the filter body 202.

Figure 2B is a schematic representation of a side view of another embodiment of a filter 220 in accordance with the present invention. The filter 220 has a shape and size that is defined by a filter body 222 having an interconnected square pattern. As shown, the filter body 222 is in the shape of an extended double funnel filter. That is, the filter body 222 is shaped substantially similarly to extended two funnels 228, 230 that have tubes 224, 226 coupled to the wide portion of the funnels 228, 230 that are in turn coupled together at the median point 232. The various features of the filter body 220 can be configured similarly to the filter 100 of Figure IA or another embodiment of a filter described herein. Accordingly, the first funnel 228 can have an opening that allows a body fluid to flow therethrough with the filter body 222 having a first tube 224 that is coupled to a first funnel 228 that decreases the cross- sectional profile until reaching the median point 232. The second tube 226 and second funnel 230 may be substantially similar to the first tube 224 and first funnel 228; however, it may be oriented in the opposite direction. This may allow the filter 220 to be bi-directional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid.

Figure 2B also shows first wall contacts 221a,b to be disposed on the first tube 224, and being coupled thereto via fasteners 223a-d. Also, second wall contacts 227a,b are shown to be disposed on and coupled to the second tube 226 via fasteners 225a,b. The wall contacts 221, 227 are shown to have an outer surface configured to conform to the wall of body lumen to provide a contact surface therewith, and to have an inner surface configured to conform to the outer surface of the tubes 224, 226 of the filter body 222. Figure 2C is a schematic representation of a side view of another embodiment of a filter 240 in accordance with the present invention. The filter 240 has a shape and size that is defined by a filter body 242 having an interconnected sinusoidal pattern. As shown, the filter body 242 is in the shape of a double funnel filter with a conduit median 248 disposed between a first funnel 244 and a second funnel 246. That is, the filter body 242 is shaped substantially similarly to two funnels 244, 246 that are coupled together with a median conduit 248. The various features of the filter body 242 can be configured similarly to the filter 100 of Figure IA or another embodiment of a filter described herein. Accordingly, the first funnel 244 can have an opening that allows a body fluid to flow therethrough with the filter body 242 forming a funnel that decreases the cross-sectional profile until reaching the median conduit 248, which can have any shape and size to filter selected particulate sizes from the body fluid. The second funnel 246 may be substantially similar to the first funnel 244; however, it may be oriented in the opposite direction on the other side of the median conduit 248. This may allow the filter 240 to be bi-directional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid.

Figure 2C also shows a first wall contact 241a to be disposed on a first side of the filter body 242, and a second wall contact 241b to be disposed on a second side of the filter body 242. The first and second wall contacts 241a,b may be coupled to the filter body 242 via fasteners 243a-d. The wall contacts 241a,b are shown to have an outer surface configured to conform with the wall of a body lumen to provide a contact surface therewith, and to have an inner surface configured to conform with the shape of the outer surface of the filter body 242.

Figure 2D is a schematic representation of a side view of another embodiment of a filter 260 in accordance with the present invention. The filter 260 has a shape and size that is defined by a filter body 262 having a checkerboard pattern. As shown, the filter body 262 is in the shape of a tube that has a parabolically narrowed central region. That is, the filter body 262 is shaped substantially similarly to two tubes 264, 266 that are coupled together at a parabolic median 268. The various features of the filter body 262 can be configured similarly to the filter 100 of Figure IA or another embodiment of a filter described herein. Accordingly, the first tube 264 can have an opening that allows a body fluid to flow therethrough with the filter body 262 having a parabolic median 268 that decreases the cross-sectional profile until reaching a central point, and then the parabolic median 268 increases in cross-sectional profile until reaching the second tube 266. The second tube 266 may be substantially similar to the first tube 264; however, it may be oriented in the opposite direction. This may allow the filter 260 to be bidirectional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid. Figure 2D also shows wall contacts 261a,b to be disposed on the filter body 262, and being coupled thereto via fasteners 263a-d. The wall contacts 261a,b are shown to have an outer surface configured to conform with the wall of a body lumen to provide a contact surface therewith, and to have an inner surface configured to conform with the outer surface of the tubes 264, 266 of the filter body 262. As shown, the wall contacts 261a,b have a length commensurate with the length of the entire filter body 262. As such, the wall contacts 261a,b may extend from the first portion 264 over the parabolic portion 268 and/or across the second portion 266.

Figures 3A-3D illustrate schematic representations of embodiments of the substantially cone-shaped filter portion of an endoprosthesis in accordance with the present invention. As illustrated, the cone-shaped filter portion can have different configurations in order to filter or selectively filter particulates from a body fluid in a body lumen.

Figure 3A illustrates an embodiment of a substantially funnel-shaped filter 300 in accordance with the present invention. As shown, the funnel-shaped filter 300 has a twisted funnel-shaped body 301 that is shaped by structural elements 303 (i.e., filter elements) that cooperate to form the filter 300. The funnel-shaped filter 300 is illustrated to show the features of the filter 300 between the funnel large end 302 and the funnel small end 304. The structural elements 303 may be formed by a plurality of radial members 306 that spiral between the funnel small end 304 and the funnel large end 302. As such, the radial members 306 may cooperatively form apertures 310 that may increase in cross section between the funnel small end 304 and the funnel large end 302. The smaller cross section at the funnel small end 304 may allow for the filtering of smaller particles in the body fluid and/or the larger cross section at the funnel large end 302 may allow for similarly sized particles to pass therethrough. The apertures 310 may thereby inhibit larger particles near the funnel small end 304 and allow smaller particles to pass through near the funnel large end 302. Optionally, the funnel-shaped filter 300 can include circular members 308 as shown by the dashed lines. The circular members 308 can cooperate with the radial members 306 to form much smaller apertures 310 that are configured similarly to pores of standard filters. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and/or which particles will be allowed to pass through the filter 300 and continue flowing in the body lumen.

Additionally, Figure 3A shows four wall contacts 305a-d being evenly disposed about the circumference of the filter body 301. Each of the wall contacts 305a-d may be coupled to the filter body 301 via fasteners 307a-d. The outer surface of each of the wall contacts 305a-d may be curved to conform to the inner surface of a body lumen, and/or the inner surface of each of the wall contacts 305a-d may be curved to conform to the outer surface of the filter body 301. Figure 3B illustrates an embodiment of a substantially funnel-shaped filter 320 in accordance with the present invention. As shown, the funnel-shaped filter 320 has a target- shaped body 321 that is shaped by structural elements 323 that cooperate to form the filter 320. The funnel-shaped filter 320 is illustrated to show the features of the filter 320 between the funnel large end 322 and the funnel small end 324. The structural elements 323 may be formed by a plurality of radial members 326 that may extend substantially linearly or straight without spiraling between the funnel small end 324 and the funnel large end 322. As such, the radial members 326 may cooperatively form apertures 340 that may increase in cross section between the funnel small end 324 and the funnel large end 322. The smaller cross section at the funnel small end 324 may facilitate the filtering of smaller particles in the body fluid and/or the larger cross section at the funnel large end 322 may facilitate similarly sized particles to pass therethrough. The apertures 340 may thereby inhibit larger particles near the funnel small end 324 and may allow smaller particles to pass through near the funnel large end 322. As shown, the funnel-shaped filter 320 includes circular members 328. The circular members 328 may cooperate with the radial members 326 to form much smaller apertures 340 that are configured similarly to pores of standard filters. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 300 and continue flowing in the body lumen.

Additionally, Figure 3B shows two wall contacts 325a,b disposed on the outer surface of the filter body 321 opposite from each other. Each of the wall contacts 325a,b may be coupled to the filter body 321 via fasteners 327a,b. The outer surface of each of the wall contacts 325a,b may be flat to apply differential pressure to the inner surface of a body lumen, which may allow the wall contacts 325a,b to degrade and/or then to conform to the inner surface of the body lumen. The inner surface of each of the wall contact 325a,b may be curved to conform to the outer surface of the filter body 321.

Figure 3C illustrates an embodiment of a substantially funnel-shape filter 350 in accordance with the present invention. As shown, the funnel-shaped filter 350 has a checkerboard-shaped body 351 that is shaped by structural elements 353 that cooperate to form the filter 350. The funnel-shaped filter 350 is illustrated to show the features of the filter 350 between the funnel large end 352 and the funnel small end 354. The structural elements 353 may be formed by a plurality of vertical members 356 and/or a plurality of horizontal members 358 that may cooperatively form apertures 360 that may be substantially the same size between the funnel small end 354 and the funnel large end 352. The substantially similar apertures 360 at the funnel small end 354 and funnel large end 352 may allow for the filtering of the same sized particles in the body fluid so that there is a size exclusion cutoff size. Accordingly, same sized apertures 360 may thereby inhibit the same size particles near the funnel small end 354 and the funnel large end 352. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 350 and continue flowing in the body lumen.

Additionally, Figure 3C shows two wall contacts 355a,b being disposed on the outer surface of the filter body 351 opposite from each other. Each of the wall contacts 355a,b may be coupled to the filter body 351 via fasteners 357a,b. The outer surface of each of the wall contacts 355a,b may be flat, and the inner surface of each of the wall contact 355a,b may also be flat. The wall contacts 355a,b may be made from a malleable and/or flexible material that allows the wall contacts 355a,b to bend to conform with the inner surface of the body lumen and/or the outer surface of the filter body 351.

Figure 3D illustrates an embodiment of a substantially funnel-shape filter 370 in accordance with the present invention. As shown, the funnel-shaped filter 370 has a wheel spoke-shaped body 371 that is shaped by structural elements 373 that cooperate to form the filter 370. The funnel-shaped filter 370 is illustrated to show the features of the filter 370 between the funnel large end 372 and the funnel small end 374. The structural elements 373 may be formed by a plurality of radial members 376 that may extend substantially linearly and/or straight without spiraling from the funnel small end 374 to the funnel large end 372. As such, the radial members 376 may cooperatively form apertures 378 that may increase in cross section from the funnel small end 374 to the funnel large end 372. The smaller cross section at the funnel small end 374 may allow for the filtering of smaller particles in the body fluid and/or the larger cross section at the funnel large end 372 may allow for similarly sized particles to pass therethrough. The apertures 378 may thereby inhibit larger particles near the funnel small end 374 and/or may allow smaller particles to pass through near the funnel large end 372. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 370 and continue flowing in the body lumen.

Additionally, Figure 3D shows two wall contacts 375a,b being disposed on the outer surface of the filter body 371 opposite and from each other because they cooperate to form an outer tubular shape that extends around the circumference of the filter body 371. Each of the wall contacts 375a,b may be coupled to the filter body 371 via fasteners 377a,b. The body of each wall contact 375a,b may be configured as a half tube so that the combined outer surface of the wall contacts 375a,b forms a tube that may conform to the shape of the inner surface of a body lumen. The inner surface of each of the wall contacts 375a,b may also be a half tube so that the combined inner surface area of the wall contacts 375a,b circumnavigates around the entire outer surface of the filter body 371.

Figure 3E illustrates an embodiment of a filter 380 in accordance with the present invention. As shown, the filter 380 has a sectioned spiral-shaped body 381 that is shaped by structural elements 383 that cooperate to form the filter 380. The cone-shaped filter 380 is illustrated to show the features of the filter 380 between the funnel large end 382 and the funnel small end 384. The structural elements 383 may be formed by a single spiral member 386 that may spiral between the funnel small end 384 and the funnel large end 382. As such, the spiral member 386 may cooperatively form an aperture 390 that spirally extends and/or increases in cross section between the funnel small end 384 and the funnel large end 382. Optionally, the filter 380 can include radial members 388 as shown by the dashed lines, wherein the radial members 388 can be substantially similar to other radial members depicted in the other embodiments. The radial members 388 can cooperate with the spiral member 386 to form much smaller apertures 390 that are configured similarly to pores of standard filters. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 380 and continue flowing in the body lumen.

Additionally, Figure 3E shows a wall contact 385 that is disposed on the outer surface of the filter body 381 to form an outer tubular shape that extends around the circumference of the filter body 381. The wall contact 385 may be coupled to the filter body 381 via fasteners (not shown), affixation, coating, or other means of attaching concentric tubes. The body of the wall contact 385 may be configured as a tubular shape so that the outer surface of the wall contact 385 forms a tube that may conform to the shape of the inner surface of a body lumen. The inner surface of the wall contact 385 may also be tubular shape so that the combined inner surface area of the wall contact 385 may circumnavigate around the entire outer surface of the filter body 381.

Figure 3F illustrates an embodiment of a filter 392 in accordance with the present invention. As shown, the filter 392 has a sectioned spiral-shaped body 391 that is shaped by structural elements 393 that cooperate to form the filter 392. The cone-shaped filter 392 is illustrated to show the features of the filter 392 between the funnel large end 394 and the funnel small end 396. The structural elements 393 may be formed by a single spiral member 398 that may spiral between the funnel small end 396 and the funnel large end 394. As such, the spiral member 398 may cooperatively form an aperture 399 that spirally extends and increases in cross section between the funnel small end 396 and the funnel large end 394. The spiral member 398 may be wound tighter near the funnel small end 396 compared to the funnel large end 394. However, the spiral member 398 can be wound tighter at the funnel large end 394 compared to the funnel small end 396, or any other variation. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 392 and continue flowing in the body lumen.

Figures 4A-4C are schematic representations of a filter 410 disposed within a body lumen 400. The body lumen 400 includes an inner surface 402 that receives the filter 410. As such, the body lumen 400 has a diameter 404 that is similar in size to the filter 410. The filter 410 can be substantially similar to any of the filters depicted and/or described herein.

As shown, the filter 410 is defined by a filter body 411 that has a first end 414 and an opposite second end 416. The first end 414 is configured for receiving a flow of body fluid within the body lumen 400, and the second end 416 is configured for filtering particulates from the body fluid and to allow the body fluid to exit the filter 410. The filter body 411 may include a fastener hole 418 that can receive a fastener 431 that may couple the wall contact 420 with the filter body 411.

The wall contact 420 may include an outer surface 422 that is configured to contact the inner surface 402 of the body lumen 400. Additionally, the wall contact 420 may include an inner surface 424 that is configured to contact the filter body 411. The wall contact 420 may have a first end 426 and an opposite second end 428. The inner surface 424 of the wall contact 420 may be configured to receive the fastener 431, wherein the fastener 431 can be permanently or removably coupled thereto. The fastener 431 may include a shaft 432 and/or a head 430. The shaft 432 may be configured to be inserted through and/or fit within the fastener hole 418. The head 430 may be configured to have a larger size than at least a portion of the fastener hole 418 so that the head 430 can be positioned not to slide into the fastener hole 418, which functions to hold the fastener 431 in position and couple the wall contact 420 with the filter body 411.

Figure 4B shows a first fastener 431a and a second fastener 431b coupling a wall contact 420a to the filter body 411a. The filter body 411a may include a first fastener hole 418a that may receive the first shaft 432a so that the first head 430a holds the wall contact 420a to the filter body 411a. Additionally, the filter body 411a may include a second fastener hole 418b that may receive the second shaft 432b of the second fastener 431b so that the second head 430b holds the wall contact 420a to the filter body 411a. In the instance the fasteners 431a,b are permanently affixed to the wall contact 420a, a portion of the fastener holes 418a,b may be at least as large as the fastener heads 430a,b so that they can fit therethrough during the process of coupling the wall contact 420a with the filter body 41 Ia.

Figure 4C is a schematic representation of one embodiment of a filter body 411a that is configured to removably receive a wall contact 420a. As such, the filter body 411a may include fastener holes 418a,b being formed into the shape of a keyway slot. The keyway slot shape of the fastener holes 418a,b may have a large opening portion 417a,b that is large enough to receive the fastener head 430a,b therethrough. Additionally, the keyway slot shape of the fastener holes 418a,b may have a small opening portion 419a,b that is small enough to inhibit the fastener head 430a,b from moving into the fastener hole 418a,b, but is large enough to receive the fastener shaft 432a,b therein. The keyway slot shape configuration may thereby allow the fastener 431a,b to be inserted through the large opening portion 417a,b and then allows the fastener shaft 432a,b to be slipped or otherwise passed into the small opening portion 419a,b so that the fastener head 430a,b is disposed on the inner surface of the filter body 411a to securely hold the wall contact 420a against the external surface of the filter body 411a. The size of the aperture or apertures, which function as pores, can be dimensioned as needed for different applications. As such, the aperture or apertures can have smaller dimensions when the filter is designed to filter out smaller particulates. Conversely, the aperture or apertures can have larger dimensions when smaller particulates are needed to be filtered, but the apertures or apertures still filter out particles larger than the cutoff dimension. For example the apertures can have a dimension ranging from about 0.00001 mm to about 0.1 mm, from about 0.0001 mm to about 0.01 mm, and/or from about 0.001 mm to about 0.001 mm.

The size, shape, and number of the wall contacts for a given filter can be modulated as needed for different applications. The wall contacts can have smaller dimensions when used in smaller vessels. Conversely, the wall contacts can have larger dimensions when used in larger vessels For example, the wall contacts can have a thickness that can range from about 0.00001 mm to about 1 mm, from about 0.0001 mm to about 0.1 mm, and/or from about 0.001 mm to about 0.01 mm. The wall contacts can have a width that can range from 0.00001 mm to about 1 mm, from about 0.0001 mm to about 0.1 mm, and/or from about 0.001 mm to about 0.01 mm. The wall contacts can have a longitudinal length that can range from about 0 mm to about 50 mm, from about 0.001 to about 25 mm, and/or about 0.1 mm to about 10 mm.

The fasteners of the present invention can be configured as any standard fastener used in the medical arts to attach one medical component to another medical component. Such fasteners can be in the form of an adhesive, screw, nail, cotter pin, bolts, nuts, and the like. The fastener can be the same or similar material as the filter and/or the wall contact or a different material. The fastener can be integrated, permanently coupleable, or removably coupleable with the wall contact. For example, the fastener system can include the wall contact having a bolt-like protrusion extending through the fastener hold of the filter with a nut securing the wall contact to the filter by being fitted onto the bolt- like protrusion. In another example, the fastener is substantially a nail-like structure integrated with the wall contact or formed therewith. In yet another example, the fastener is a screw that fits through the fastener hole and into the wall contact, where the screw head is larger than at least a portion of the fastener hole. In still yet another example, the wall contact includes a recess, such as a threaded recess, to receive the fastener.

Additionally, a filter can have at least one wall contact. For example, the filter can have one wall contact that extends around the entire circumference of the external surface of the filter. The filter can have two wall contacts that are disposed oppositely from each other. The filter can have 3, 4, 5, or more wall contacts that are distributed around the circumference and/or the longitudinal axis of the external surface of a filter. The filter can have wall contacts that are adjacent and/or touching to extend partially through fully around the entire circumference of the external surface of the filter. Figure 6A is a schematic representation of a filter 610 having a central axis 676, which is shown in side a view, in accordance with the present invention. The filter 610 may have an hourglass-like shape that is defined by the body 612, which includes a first body portion 620, second body portion 632, first funnel body 644, second funnel body 656, and median body 668. The filter 610 may be arranged such that the first body portion 620 is coupled to the first funnel body 644, which is coupled to the median body 668, which is coupled to the second funnel body 656, which is coupled to the second body portion 632. The body 612 can include of a plurality of filter structural elements 614 (e.g., strut element, braids, or the like) that may cooperate to provide structural integrity to the filter 610. The body 612 and/or structural elements 614 can be shaped and/or otherwise configured similarly to an endoprosthesis configured for deployment into a body lumen, examples of which include lumen filters, stents, and the like. The structural elements 614 may include annular elements, helical elements, crossbars, connectors, junctions, braids, and other like features. The hourglass shape of the body 612 may at least partially define a first end 616 that includes a first opening 618 formed therein. The first end 616 is disposed at a longitudinal end of the body 612, and the first opening 618 can be substantially the same dimensions as the first end 616. The segment of the body 612 that defines the first end 616 is the first body portion 620. The first body portion 620 can have various shapes and sizes; however, it is depicted as being substantially cylindrical in Figure 6A. The first body portion 620 defines a first large conduit 622 that is fluidly coupled with the first opening 618 such that an object can pass through the first opening 618 and into the first large conduit 622, or vice versa. The first large conduit 622 has a first large diameter 624 that has a uniform or varying dimension. The first large diameter 624 can be substantially uniform such that the first body portion 620 has a substantially uniform cross-sectional profile. The first body portion 620 and/or the first large conduit 622 has a first length 626 that extends from the first end 616 and/or first opening 618 to the opposite end of the first body portion 620 and/or first large conduit 622.

Additionally, the opposite end of the hourglass shape of the body 612 from the first end 616 may at least partially define a second end 628 that includes a second opening 630 formed therein. The second end 628 is disposed at a longitudinal end of the body 612, and the second opening 630 can be substantially the same dimensions as the second end 628. The segment of the body 612 that defines the second end 628 is the second body portion 632. The second body portion 632 can have various shapes and sizes; however, it is depicted as being substantially cylindrical in Figure 6A, which is similar to the first body portion 620. The second body portion 632 defines a second large conduit 634 that is fluidly coupled with the second opening 630 such that an object can pass through the second opening 630 and into the second large conduit 634, or vice versa. The second large conduit 634 has a second large diameter 636 that has a uniform or varying dimension. The second large diameter 636 can be substantially uniform such that the second body portion 632 has a substantially uniform cross-sectional profile. The second body portion 632 and/or the second large conduit 634 has a second length 638 that extends from the second end 628 and/or second opening 630 to the opposite end of the second body portion 632 and/or second large conduit 634.

The first body portion 620 may be fluidly coupled with a first funnel body 644 such that the end of the first body portion 620 opposite of the first end 616 and/or first opening 618 is coupled to the first funnel large end 640. As such, the first funnel large end 640 can be considered to be a junction with the first body portion 620. The first funnel body 644 may also have a first funnel small end 642 that is opposite of the first funnel large end 640. As shown, the first funnel large end 640 has a larger diameter and/or opening compared to the first funnel small end 642. The first funnel body 644 defines a first funnel conduit 650 which is disposed therein. The first funnel body 644 and/or first funnel conduit 650 includes a first funnel diameter 646 that decreases from the first funnel large end 640 to the first funnel small end 642 such that the cross-sectional profile of the first funnel body 644 and/or first funnel conduit 650 correspondingly decreases. The first funnel body 644 and/or the first funnel conduit 650 has a first funnel length 648 that extends from the first funnel large end 640 to the opposite first funnel small end 642. The second body portion 632 may be fluidly coupled with a second funnel body

656 such that the end of the second body portion 632 opposite of the second end 628 and/or second opening 630 is coupled to the second funnel large end 652. As such, the second funnel large end 652 can be considered to be a junction with the second body portion 632. The second funnel body 656 also has a second funnel small end 654 that is opposite of the second funnel large end 652. As shown, the second funnel large end 652 has a larger diameter and/or opening compared to the second funnel small end 654. The second funnel body 656 defines a second funnel conduit 662 which is disposed therein. The second funnel body 656 and/or second funnel conduit 662 includes a second funnel diameter 658 that decreases from the second funnel large end 652 to the second funnel small end 654 such that the cross-sectional profile of the second funnel body 656 and/or second funnel conduit 662 correspondingly decreases. The second funnel body 656 and/or the second funnel conduit 662 has a second funnel length 660 that extends from the second funnel large end 652 to the opposite second funnel small end 654. The first funnel small end 642 of the first funnel body 644 may be coupled to the first median end 664 of the median body 668, and/or the second funnel small end 654 of the second funnel body 656 may be coupled to the second median end 666 of the median body 668. This configuration may dispose the median body 668 between the first funnel body 644 and the second funnel body 656. The median body 668 defines a median conduit 674 having a median diameter 670 and a median length 672. The median diameter 670 can have a dimension that is substantially the same from the first median end 664 to the second median end 666, or the dimension can be varied, such as increasing, decreasing, parabolic, and the like.

The filter 610 can be configured such that each corresponding portion along the central axis 676 is similar or different. For example, the first body portion 620 can have shapes and/or dimensions that are the same or different from the shapes and/or dimensions of the second body portion 632. The first funnel body 644 can have shapes and/or dimensions that are the same or different from the shapes and/or dimensions of the second funnel body 656. Also, the median body 668 can be configured such that the median conduit 674 is sufficiently small to inhibit blood clot particulates. This may allow the filter 610 to filter the blood. Also, the first length 626 of the first body portion 620 and/or the second length 638 of the second body portion 632 can be dimensioned to improve the static disposition of the filter 610 within a body lumen such that the filter 610 may be substantially immobile after deployment. This can impart an enlarged contact surface area with the body lumen that may allow the filter 610 to have increased contact with the body lumen. Additionally, the first funnel length 648 and/or second funnel length 660 can be dimensioned to improve the filtering capability of the filter 610, wherein such dimension changes can include sharper or more gradual slopes of the conical shape. Moreover, the dimensions of the median body 668 can be modulated to change the filtering characteristics of the filter 610, where a smaller median conduit 674 can catch smaller particles and a larger median conduit 674 can allow larger particles to pass therethrough. Thus, the diameter, shape, length, other characteristics, or combinations thereof of the median conduit 674 can be tailored for a particular body lumen and/or for the size of particulates to be captured and filtered from the body fluid. For example, the large diameters 624, 636 can be from about 0.001 mm to about 10 mm, from about 0.01 mm to about 5 mm, and/or about 0.1 mm to about 1 mm. The lengths 626, 638 can be from about 0 mm to about 50 mm, about 0.001 to about 25 mm, and/or about 0.1 mm to about 10 mm. The funnel diameters 646, 658 can be from about 0 mm to about 10 mm, from about 0.001 mm to about 5 mm, and/or about 0.01 mm to about 1 mm. The funnel lengths 648, 660 can be from about 0.01 mm to about 50 mm, from about 0.1 mm to about 25 mm, and/or about 0.5 mm to about 1 mm. The median diameter 670 can be from about 0 mm to about 1 mm, from about 0.0001 mm to about 0.5 mm, and/or about 0.001 mm to about 0.01 mm. The median length 672 can be from about 0 mm to about 50 mm, from about 0.001 mm to about 25 mm, and/or about 0.01 mm to about 10 mm. However, other sizes can be employed and determined by routine studies of the vasculature or other body lumen in which the filter will be placed.

Figure 6B is a schematic representation of a cross-sectional profile of the filter 610 taken at lines B shown in Figure 6A, which mainly depicts the cross-sectional profile of the first body portion 620, the first funnel body 644, and the median conduit 674. As shown, the first body portion 620 has a first large diameter 624 that is substantially similar to the size of the first funnel large end 640. The first funnel body 644 narrows the first funnel conduit 650 until reaching the small opening of the median conduit 674, which has a small median diameter 670. The first funnel body 644 can include a plurality of structural elements 614 that cooperate to form filter apertures 615 (i.e., apertures) that are substantially filter pores. The size and/or shapes of the filter apertures 615 can be configured to be larger or smaller depending on the size of particulates to be trapped and filtered from the body fluid. For example the filter apertures 615 can have a dimension ranging from about 0.00001 mm to about 0.1 mm, from about 0.0001 mm to about 0.01 mm, and/or from about 0.001 mm to about 0.001 mm.

Figures 6A-6B also show an example of an embodiment of the configuration of the structural elements 614 and the corresponding filter apertures 615. As shown, the filter apertures 615 proximate to the first funnel large end 640 have substantially the same dimensions as the filter apertures 615 that are proximate to the first funnel small end 642. However, the filter apertures 615 proximate to the first funnel large end 640 can be larger than the filter apertures 615 that are proximate to the first funnel small end 642, or vice versa. However, the filter apertures 615 can have any functional shape and/or size to function as a filter pore. Figures 7A-7D illustrate schematic representations of additional embodiments of an endoprosthesis in accordance with the present invention. As illustrated, the endoprosthesis can be configured into a filter for a body lumen.

Figure 7A is a schematic representation of a side view of a filter 700 in accordance with the present invention. The filter 700 has a shape and size that is defined by a filter body 702 having an interconnected diamond pattern. As shown, the filter body 702 is in the shape of a double funnel filter. That is, the filter body 702 may be shaped substantially similarly to two funnels 704, 706 that are coupled together at the median point 708 (e.g., median conduit). The various features of the filter body 702 can be configured similarly to the filter 610 of Figure 6 A or any other embodiment of a filter described herein. Accordingly, the first funnel 704 can have an opening that allows a body fluid to flow therethrough with the filter body 702 that decreases the cross-sectional profile until reaching the median point 708. The second funnel 706 may be substantially similar to the first funnel 704; however, it may be oriented in the opposite direction. This may allow the filter 700 to be bidirectional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid.

Figure 7B is a schematic representation of a side view of another embodiment of a filter 720 in accordance with the present invention. The filter 720 may have a shape and size that is defined by a filter body 722 having an interconnected square pattern. As shown, the filter body 722 is in the shape of an extended double funnel filter. That is, the filter body 722 is shaped substantially similarly to two extended funnels 728, 730 that have tubes 724, 726 coupled to the wide portion of the funnels 728, 730 that are in turn coupled together at the median point 732. The various features of the filter body 720 can be configured similarly to the filter 610 of Figure 6 A or any other embodiment of a filter described herein. Accordingly, the first funnel 728 can have an opening that allows a body fluid to flow therethrough with the filter body 722 having a first tube 724 that is coupled to a first funnel 728 that may decrease the cross-sectional profile until reaching the median point 732. The second tube 726 and second funnel 730 may be substantially similar to the first tube 724 and/or first funnel 728; however, it may be oriented in the opposite direction. This may allow the filter 720 to be bidirectional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid. Figure 7C is a schematic representation of a side view of another embodiment of a filter 740 in accordance with the present invention. The filter 740 may have a shape and size that is defined by a filter body 742 having an interconnected sinusoidal pattern. As shown, the filter body 742 may have in the shape of a double funnel filter with a median conduit 748 disposed between a first funnel filter 744 and a second funnel filter 746. That is, the filter body 742 is shaped substantially similarly to two funnels 744, 746 that are coupled together with a median conduit 748. The various features of the filter body 742 can be configured similarly to the filter 610 of Figure 6 A or any other embodiment of a filter described herein. Accordingly, the first funnel filter 744 can have an opening that allows a body fluid to flow therethrough with the filter body 742 forming a funnel that may decrease the cross-sectional profile until reaching the median conduit 748, which can have any shape and/or size to filter selected particulate sizes from the body fluid. The second funnel filter 746 may be substantially similar to the first funnel filter 744; however, it may be oriented in the opposite direction on the other side of the median conduit 748. This may allow the filter 740 to be bidirectional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid.

Figure 7D is a schematic representation of a side view of another embodiment of a filter 760 in accordance with the present invention. The filter 760 may be a shape and size that is defined by a filter body 762 having a checkerboard pattern. As shown, the filter body 762 is in the shape of a tube that has a parabolically narrowed central region. That is, the filter body 762 is shaped substantially similarly to two tubes 764, 766 that are coupled together at a parabolic median 768. The various features of the filter body 762 can be configured similarly to the filter 610 of Figure 6 A or any other embodiment of a filter described herein. Accordingly, the first tube 764 can have an opening that allows a body fluid to flow therethrough with the filter body 762 having a parabolic median 768 that may decrease the cross-sectional profile until reaching a central point, and then the parabolic median 768 may increase in cross-sectional profile until reaching the second tube 766. The second tube 766 may be substantially similar to the first tube 764; however, it may be oriented in the opposite direction. This may allow the filter 760 to be bidirectional and/or be placed in the body lumen with either end receiving the flow of body fluid, and the opposite end being the exit for the body fluid.

Figures 8A- 8D illustrate schematic representations of embodiments of the substantially funnel-shaped filter portion of an endoprosthesis in accordance with the present invention. As illustrated, the funnel-shaped filter portion can have different configurations in order to filter or selectively filter particulates from a body fluid in a body lumen.

Figure 8A illustrates an embodiment of a substantially funnel-shaped filter 800 in accordance with the present invention. As shown, the funnel-shaped filter 800 has a twisted funnel-shaped body 801 that is shaped by structural elements 803 (i.e., filter elements) that cooperate to form the funnel-shaped filter 800. The funnel-shaped filter 800 is illustrated to show the features of the filter 800 between a funnel large end 802 and the funnel small end 804. Structural elements 803 may be formed by a plurality of radial members 806 that may spiral between the funnel small end 804 and the funnel large end 802. As such, the radial members 806 may cooperatively form apertures 810 that increase in cross section between the funnel small end 804 and the funnel large end 802. The smaller cross section of the apertures 810 at the funnel small end 804 may allow for the filtering of smaller particles in the body fluid and/or the larger cross section of the apertures 810 at the funnel large end 802 may allow for similarly sized particles to pass therethrough. The apertures 810 may thereby inhibit larger particles near the funnel small end 804 and allow smaller particles to pass through near the funnel large end 802. Optionally, the funnel-shaped filter 800 can include circular members 808 as shown by the dashed lines. The circular members 808 can cooperate with the radial members 806 to form much smaller apertures 810 that are configured similarly to pores of standard filters. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 800 and continue flowing in the body lumen.

Figure 8B illustrates an embodiment of a substantially funnel-shaped filter 820 in accordance with the present invention. As shown, the funnel-shaped filter 820 has a target- shaped body 821 that is shaped by structural elements 823 that cooperate to form the filter 820. The funnel-shaped filter 820 is illustrated to show the features of the filter 820 between funnel large end 822 and funnel small end 824. The structural elements 823 may be formed by a plurality of radial members 826 that may extend substantially linearly or straight without spiraling between the funnel small end 824 and the funnel large end 822. As such, the radial members 826 may cooperatively form apertures 840 that may increase in cross section between the funnel small end 824 and the funnel large end 822. The smaller cross section of the apertures 840 at the funnel small end 824 may allow for the filtering of smaller particles in the body fluid and/or the larger cross section at the funnel large end 822 may allow for similarly sized particles to pass therethrough. The apertures 840 may thereby inhibit larger particles near the funnel small end 824 and/or may allow smaller particles to pass through near the funnel large end 822. As shown, the funnel-shaped filter 820 includes circular members 828. The circular members 828 may cooperate with the radial members 826 to form smaller apertures 840 that may be configured similarly to pores of standard filters. This may allow for size- exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 800 and continue flowing in the body lumen. Figure 8C illustrates an embodiment of a substantially funnel-shaped filter 850 in accordance with the present invention. As shown, the funnel-shaped filter 850 has a checkerboard-shaped body 851 that is shaped by structural elements 853 that cooperate to form the filter 850. The funnel-shaped filter 850 is illustrated to show the features of the filter 850 between the funnel large end 852 and the funnel small end 854. The structural elements 853 may be formed by a plurality of vertical members 856 and/or a plurality of horizontal members 858 that may cooperatively form apertures 860 that are substantially the same size between the funnel small end 854 and the funnel large end 852. The substantially similar apertures 860 at the funnel small end 854 and funnel large end 852 may allow for the filtering of the same sized particles in the body fluid so that there is a size exclusion cutoff size. Accordingly, same sized apertures 860 may thereby inhibit the same size particles near the funnel small end 854 and the funnel large end 852. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 850 and continue flowing in the body lumen. Figure 8D illustrates an embodiment of a substantially funnel-shaped filter 870 in accordance with the present invention. As shown, the funnel-shaped filter 870 has a wheel spoke-shaped body 871 that is shaped by structural elements 873 that cooperate to form the filter 870. The funnel-shaped filter 870 is illustrated to show the features of the filter 870 between the funnel large end 872 and the funnel small end 874. The structural elements 873 may be formed by a plurality of radial members 876 that may extend substantially linearly or straight without spiraling between the funnel small end 874 and the funnel large end 872. As such, the radial members 876 may cooperatively form apertures 878 that may increase in cross section between the funnel small end 874 and the funnel large end 872. The smaller cross section of the apertures 878 at the funnel small end 874 may allow for the filtering of smaller particles in the body fluid and/or the larger cross section of the apertures 878 at the funnel large end 872 may allow for similarly sized particles to pass therethrough. The apertures 878 may thereby inhibit larger particles near the funnel small end 874 and/or allow smaller particles to pass through near the funnel large end 872. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 870 and continue flowing in the body lumen.

Figure 8E illustrates an embodiment of a substantially funnel-shaped filter 880 in accordance with the present invention. As shown, the funnel-shaped filter 880 has a sectioned spiral-shaped body 881 that is shaped by structural elements 883 that cooperate to form the filter 880. The funnel-shaped filter 880 is illustrated to show the features of the filter between the funnel large end 882 and the funnel small end 884. The structural elements 883 may be formed by a single spiral member 886 that may spiral between the funnel small end 884 and the funnel large end 882. As such, the spiral member 886 may cooperatively form an aperture 890 that may spirally extend and/or increase in cross section between the funnel small end 884 and the funnel large end 882. Optionally, the funnel-shaped filter 880 can include radial members 888 as shown by the dashed lines, wherein the radial members 888 can be substantially similar with other radial members depicted in the other embodiments. The radial members 888 can cooperate with the spiral member 886 to form much smaller apertures 890 that may be configured similarly to pores of standard filters. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 880 and continue flowing in the body lumen.

Figure 8F illustrates an embodiment of a substantially funnel-shaped filter 892 in accordance with the present invention. As shown, the funnel-shaped filter 892 has a sectioned spiral-shaped body 891 that is shaped by structural elements 893 that cooperate to form the filter 892. The funnel-shaped filter 892 is illustrated to show the features of the filter between the funnel large end 894 and the funnel small end 896. The structural elements 893 may be formed by a single spiral member 898 that may spiral between the funnel small end 896 and the funnel large end 894. As such, the spiral member 898 may cooperatively form an aperture 899 that may spirally extend and/or increase in cross section between the funnel small end 896 and the funnel large end 894. This is because the spiral member 898 may be wound tighter at the funnel small end 896 compared to the funnel large end 894. However, the spiral member 898 can be wound tighter at the funnel large end 894 compared to the funnel small end 896, or any other variation. This may allow for size-exclusion selection of which particles will be filtered from the body fluid and which particles will be allowed to pass through the filter 892 and continue flowing in the body lumen. The filter can be inserted into the vessel through a catheter or other similar type device in a compressed or flattened form, where the filter expands in the body lumen, such that the maximum diameter of the larger end portions or the wall contacts disposed on the external surface of the filter contact the vessel to stabilize and secure the position of the filter within the body lumen. Such a compressed or flattened delivery configuration can be achieved by pulling apart, increasing the axial distance between, the filter ends. This longitudinally stretches and radially compresses the filter. In this manner, the maximum diameter sections of each of the larger ends are drawn radially toward the central longitudinal axis. Upon deployment and setting, the material properties of the filter expand, drawing together, decreasing the axial distance between, the filter ends. This longitudinally compresses and radially expands the filter. In this manner, the maximum diameter end sections of the filter are radially expanded toward the vessel wall such that the wall contacts are positioned against the vessel wall. It is contemplated that the filter can be inserted either through a femoral or jugular approach as previously described. However, the filter can be configured for placement in almost any vessel or other body lumen.

To adequately hold the filter in place, the wall contacts can be disposed on the larger diameter ends of the filter to exert a radial force normal to the vena cava walls. The strut elements, and thereby the larger diameter ends, may be sufficiently resilient to be compressed into the introducer catheter and to regain their original shape after being released.

III. Deploying Filter

The filters of the present invention are configured for use in a body lumen to filter the body fluid that flows through the body lumen. This can filter particulates that are larger than a selected size from the body fluid. As such, the present invention includes a method of delivering a lumen filter into a body lumen of a subject. Such a method may include: providing a lumen filter as described herein, orienting the filter into a delivery orientation by longitudinally elongating the filter body such that the larger ends filter have a reduced dimension with a cross section that is smaller than the body lumen, inserting the filter in the delivery orientation into a delivery device, such as a deliver catheter that can be configured substantially as a catheter for delivering a lumen filter, delivering the elongated filter body to a desired deployment site within the body lumen of the subject, removing the filter from the delivery device, and longitudinally shortening the filter body such that the larger ends of the filter each have an enlarged dimension that applies radial forces to an inner wall of the body lumen.

Figure 5A is a schematic representation illustrating a delivery system 500 for delivering a filter 520a into a body lumen 540, such as a blood vessel like the vena cava. The delivery system 500 includes an endoprosthesis delivery catheter 502 configured for delivering a filter 520a that is retained by the delivery catheter 502 in a delivery orientation (e.g., longitudinally elongated and/or radially compressed). The delivery catheter 502 may include a delivery member 504 that defines a delivery lumen 507 that is shaped and dimensioned to retain the filter 520a in the delivery orientation. Accordingly, the delivery member 504 is substantially tubular and configured similarly as any delivery catheter member. An internal surface 506 defined by the delivery member 504 holds the filter 520a within the delivery catheter 502.

The filter 520a is substantially as shown in Figure 5A, and includes a body 522 having a first large portion 524 coupled to a first funnel 528 that is coupled to a second funnel 530 through an intermediate portion 532, wherein the second funnel 530 is coupled to a second large portion 526 to form the free recovery form. The first wall contacts 521a,b are shown disposed on the first large portion 524, and are coupled thereto via fasteners 523a-d. Also, second wall contacts 527a,b are shown to be disposed on and coupled to the second large portion 526 via fasteners 525a,b.

The delivery system 500 delivers the filter 520a with a delivery catheter 502 similarly to the method of delivering other endoprostheses into a body lumen. As such, an insertion site (not shown) is formed through the skin (not shown) that traverses into a body lumen 540. A guidewire (not shown) is then inserted through the insertion site, through the body lumen 540, to the delivery site 544. A catheter (not shown) is then inserted into the body lumen 540 to the delivery site 544 over the guidewire, and the guidewire is optionally extracted. The delivery catheter 502 is then inserted through the catheter (not shown) until reaching the delivery site 544 and the catheter (not shown) is withdrawn.

Optionally, the catheter is the delivery catheter 502, and in this instance, the delivery catheter 502 is retained at the delivery site 544 and the filter 520a is delivered to the delivery site 544 through the lumen 507 of the delivery catheter 502. A pusher 510 can be used to push the filter 520a within the lumen 507 of the delivery catheter 502 to the delivery site 544.

Accordingly, the delivery system 500 is inserted through percutaneous insertion site (not shown) that traverses from the skin (not shown) into the body lumen 540 until reaching the delivery site 544. The pusher 510 includes a distal end 512 that pushes the filter 520a from the distal end 508 of the delivery member 504. This is shown by the arrow pointing toward the distal end 508 of the delivery member 504, which shows the relative movement of the pusher 510 and thereby the filter 520a relative to the delivery member 504 and body lumen 540. Alternatively, the filter 520a can be disposed at the distal end 508 of the delivery member 504, and the pusher 510 holds the filter 520a at the delivery site 544 and the delivery member 504 is retracted over the filter 520a and pusher 510, which is shown by the arrows. Thus, the pusher 510 can push the filter from the delivery catheter 502 or the delivery member 504 can be withdrawn over the filter 520a and pusher 510 in order to deploy the filter 520a. Figure 5B illustrates a filter 520b in the deployed configuration at the delivery site

544 within the body lumen 540. As such, the filter 520 is longitudinally shortened and radially expanded to contact the inner wall 542 of the body lumen 540.

Figure 9A is a schematic representation illustrating a delivery system 900 for delivering a filter 920a into a body lumen 940, such as a blood vessel like the vena cava. The filter 920a may include a body 922 having a first large portion 924 coupled to a first funnel 928 that is coupled to a second funnel 930 through an intermediate portion 932, wherein the second funnel 930 is coupled to a second large portion 926 to form the free recovery form. The delivery system includes an endoprosthesis delivery catheter 902 configured for delivering a filter 920a that is retained by the delivery catheter 902 in a delivery orientation (e.g., longitudinally elongated and radially compressed). The delivery catheter 902 includes a delivery member 904 that defines a delivery lumen 907 that is shaped and dimensioned to retain the filter 920a in the delivery orientation. Accordingly, the delivery member 904 is substantially tubular and configured similarly as any delivery catheter member. An internal surface 906 defined by the delivery member 904 holds the filter 920a within the delivery catheter 902.

The delivery system 900 delivers the filter 920a with delivery catheter 902 similarly to the method of delivering other endoprostheses into a body lumen. As such, an insertion site (not shown) is formed through the skin (not shown) that traverses into a body lumen 940. A guidewire (not shown) is then inserted through the insertion site, through the body lumen 940, to the delivery site 944. A catheter (not shown) is then inserted into the body lumen 940 to the delivery site 944 over the guidewire, and the guidewire is optionally extracted. The delivery catheter 902 is then inserted through the catheter (not shown) until reaching the delivery site 944 and the catheter is withdrawn. Optionally, the catheter is the delivery catheter 902, and in this instance, the delivery catheter 902 is retained at the delivery site 944 and the filter 920a is delivered to the delivery site 944 through the delivery lumen 907 of the delivery catheter 902. A pusher 910 can be used to push the filter 920a within the delivery lumen 907 of the delivery catheter 902 to the delivery site 944. Accordingly, the delivery system 900 is inserted through percutaneous insertion site (not shown) that traverses from the skin (not shown) into the body lumen 940 until reaching the delivery site 944. The pusher 910 includes a distal end 912 that pushes the filter 920a from the distal end 908 of the delivery member 904. This is shown by the arrow pointing toward the distal end 908 of the delivery member 904, which shows the relative movement of the pusher 910 and thereby the filter 920a relative to the delivery member 904 and body lumen 940. Alternatively, the filter 920a can be disposed at the distal end 908 of the delivery member 904, and the pusher 910 holds the filter 920a at the delivery site 944 and the delivery member 904 is retracted over the filter 920a and pusher 910, which is shown by the arrows. Thus, the pusher 910 can push the filter from the delivery catheter 902 or the delivery member 904 can be withdrawn over the filter 920a and pusher 910 in order to deploy the filter 920a.

Figure 9B illustrates a filter 920b in the deployed configuration at the delivery site 944 within the body lumen 940. As such, the filter 920b is longitudinally shortened and radially expanded to contact the inner wall 942 of the body lumen 940. In one embodiment, the present invention can include a method of extracting a filter from the body lumen, which can include: inserting a filter-extracting medical device into the body lumen to come into contact with the filter; engaging the filter-extracting medical device with the filter; longitudinally elongating the filter body such that the larger ends of the filter have a reduced dimension with a cross section that is smaller than the body lumen; and retrieving the elongated filter body from the desired deployment site within the body lumen of the subject. Optionally, the elongated filter can be received into the filter-extracting medical device, which can be substantially similar to a catheter.

In one embodiment, at least one of delivering or retrieving the filter is performed with a catheter. Catheters configured for delivering and/or retrieving endoprostheses from a body lumen can be adapted for delivering and/or retrieving the filter of the present invention.

IV. Filter Members

In one embodiment, the filter may be formed from a plurality of strut members (i.e., filter members) that are interconnected together similar to the interconnected structure of annular element, such as a stent. The members can be formed of shape memory materials (SMM), where multiple types of SMMs can be employed together in a single filter.

In one embodiment, the strut member of the filter can be formed from several wires braided together in order to produce a braided wire with a desired outer diameter. Furthermore, a single wire may be encapsulated in a multi-strand braid. The braided wires can include a combination of SMMs, such that the combination of number braided wires and elements permits a desired filter function during deployment, filtering, and extraction. In one embodiment, the body of the filter can be formed from a plurality of braided members. That is, the braided members can be substituted for the strut members, but be disposed in a braided configuration. For example, elongate members similar in form and function to the strut members can be substituted for the strut members and be fashioned together to form a braided body. Such elongate members themselves can be prepared from braided wires or other braided members that have much smaller diameters compared to the elongate members and/or strut members.

In one embodiment, the filter may be formed from a plurality of strut members that are interconnected together similar to the interconnected structure of an annular element, such as a stent. The members can be formed of shape memory materials (SMM), where multiple types of SMMs can be employed together in a single filter.

In one embodiment, each strut member can include a plurality of braided wires. The strut members can be substantially in the shape of a ribbon. That is, the strut member can have a substantially flat shape. The strut members can have a circular, oval, square, triangular, rectangular, polygonal, or other shape. In a method of manufacture, the braided wires forming the strut elements are heat set in the braid. The braided wires can be coated/jacketed with the biocompatible, biodegradable, and/or bioneutral material.

In presently described embodiments, strut elements having a rectangular, ribbon, or strip cross-sectional profile is employed, though oval-shaped or round cross-sections can also be employed. In the case of rectangular or oval cross-sections, the strut elements can be oriented so that the long dimension is parallel with and adjacent to the vena cava wall, with the narrow direction arranged radially. The thickness of the strut elements is between 0.003 and 0.015 inch and/or between 0.005 and 0.009 inch. The width of the strut element is between 0.020 and 0.045 inch and/or between 0.025 and 0.035 inch. In one embodiment, the large diameter portions of the filter can include an outer coating. The outer coating can be biocompatible, optionally biodegradable, and cover at least a portion of the large diameter portions that contact the body lumen. The coating can leave the apertures between the strut elements or braids open, or it can seal the apertures to provide a sleeve. As such, the outer coating can be configured to prevent adhesion of the tissue of the vessel to the filter. As such, the filter can be removed without substantially tearing or damaging the repaired vessel.

Furthermore, the filter, such as in the coating described above, can include a beneficial or pharmaceutical agent. The beneficial agent can include an anti-restenotic agent which decreases or prevents encapsulation of the filter with tissue growth. Exemplary anti-restenotic agents include sirolimus, everolimus, taxol, paclitaxel, and the like. Additionally, an agent can be provided which promotes healing in the vessel adjacent to the filter.

The filters of the present invention can be made of a variety of materials, such as, but not limited to, those materials which are well known in the art of endoprosthesis manufacturing. This can include, but is not limited to, a filter having a primary material for the large portions and the tapered portions. Alternatively, the tapered central portion can be made of a different material compared to the large end portions. Generally, the materials for the filter can be selected according to the structural performance and biological characteristics that are desired. In one configuration, the large end portions and/or the tapered central portions include a primary material. The large end portions and/or the tapered central portions can include resiliently flexible materials or rigid and inflexible materials. For example, materials such as Η3A12.5V, Ti6A14V, 3-2.5Ti, 6-4Ti, and platinum may be particularly good choices for adhering to a flexible material, such as, but not limited to, Nitinol and providing good crack arresting properties. The use of resiliently flexible materials can provide shock-absorbing characteristics to the large end portions and/or the tapered central portions, which can also be beneficial for absorbing stress and strains, which may inhibit crack formation at high stress zones. For example, types of materials that are used to make an endoprosthesis can be selected so that the endoprosthesis is capable of being collapsed during placement and expanded when deployed. Usually, the endoprosthesis can be self-expanding, balloon-expandable, or can use some other configuration for deployment.

In one embodiment, a filter of the present invention can include a material made from any of a variety of known suitable materials, such as a shape memory material (SMM). For example, the SMM can be shaped in a manner that allows for restriction to induce a substantially tubular, linear orientation while within a delivery shaft, but can automatically retain the memory shape of the filter once extended from the delivery shaft. SMMs have a shape memory effect in which they can be made to remember a particular shape. Once a shape has been remembered, the SMM may be bent out of shape or deformed and then returned to its original shape by unloading from strain or heating. Typically, SMMs can be shape memory alloys (SMA) including metal alloys, or shape memory plastics (SMP) including polymers.

Usually, an SMA can have any non-characteristic initial shape that can then be configured into a memory shape by heating the SMA and conforming the SMA into the desired memory shape. After the SMA is cooled, the desired memory shape can be retained. This allows for the SMA to be bent, straightened, compacted, and placed into various contortions by the application of requisite forces; however, after the forces are released, the SMA can be capable of returning to the memory shape. This can include the specific sizes of the large end portions and/or the tapered central portions. The main types of SMAs are as follows: copper- zinc-aluminium; copper-aluminium- nickel; nickel- titanium (NiTi) alloys known as nitinol; and cobalt-chromium-nickel alloys or cobalt- chromium- nickel-molybdenum alloys known as elgiloy alloys. The temperatures at which the SMA changes its crystallographic structure are characteristic of the alloy, and can be tuned by varying the elemental ratios.

For example, the primary material of a filter can be of a NiTi alloy that forms superelastic nitinol. In the present case, nitinol materials can be trained to remember a certain shape, straightened in a shaft, catheter, or other tube, and then released from the catheter or tube to return to its trained shape. This also includes the hourglass shape or the shape of the large end portions and/or the tapered central portions. Also, additional materials can be added to the nitinol depending on the desired characteristic.

A Shape Memory Plastic (SMP) can be fashioned into a filter in accordance with the present invention. When an SMP encounters a temperature above the lowest melting point of the individual polymers, the blend makes a transition to a rubbery state. The elastic modulus can change more than two orders of magnitude across the transition temperature (Ttr). As such, an SMP can form into a desired shape of a filter, braid, and/or strut element by heating it above the Ttr, fixing the SMP into the new shape, and cooling the material below Ttr. The SMP can then be arranged into a temporary shape by force, and then resume the memory shape once the force has been applied. Examples of SMPs include, but are not limited to, biodegradable polymers, such as oligo(ε- caprolactone)diol, oligo(p-dioxanone)diol, and non-biodegradable polymers such as, polynorborene, polyisoprene, styrene butadiene, polyurethane-based materials, vinyl acetate-polyester-based compounds, and others yet to be determined. As such, any SMP can be used in accordance with the present invention.

A filter having an SMM or suitable superelastic material and other suitable layers can be compressed or restrained in its delivery configuration (e.g., longitudinally elongated and radially compressed) within a delivery device using a sheath or similar restraint, and then deployed to its desired deployment configuration (e.g., longitudinally compressed and radially expanded) at a deployment site by removal of the restraint. A filter made of a thermally- sensitive material can be deployed by exposure of the filter to a sufficient temperature to facilitate expansion.

In one embodiment, the filter, braid, and/or strut element can include a variety of known suitable deformable alloy metal materials, including stainless steel, silver, platinum, tantalum, palladium, cobalt-chromium alloys or other biocompatible alloy metal materials.

In one embodiment, the filter can include a suitable biocompatible polymer in addition to or in place of a suitable metal. The polymeric filter can include biodegradable or bioabsorbable materials, which can be either plastically deformable or capable of being set in the deployed configuration. If plastically deformable, the material can be selected to allow the filter to be expanded in a similar manner using an expandable member to have sufficient radial strength and scaffolding and also to minimize recoil once expanded. If the polymer is to be set in the deployment configuration, the expandable member can be provided with a heat source or infusion ports to provide the required catalyst to set or cure the polymer. Alternative delivery devices and techniques for self-expanding endoprostheses likewise can be used. That is, the filter can be delivered and deployed much like other endoprostheses, such as stents.

Examples of such biocompatible materials for the filter can include a suitable hydrogel, hydrophilic polymer, biodegradable polymers, bioabsorbable polymers and bioneutral polymers. Examples of such polymers can include poly(alpha-hydroxy esters), polylactic acids, polylactides, poly-L-lactide, poly-DL-lactide, poly-L-lactide-co-DL- lactide, polyglycolic acids, polyglycolide, polylactic-co-glycolic acids, polyglycolide-co- lactide, polyglycolide-co-DL-lactide, polyglycolide-co-L-lactide, polyanhydrides, polyanhydride-co-imides, polyesters, polyorthoesters, polycaprolactones, polyesters, polyanydrides, polyphosphazenes, polyester amides, polyester urethanes, polycarbonates, polytrimethylene carbonates, polyglycolide-co-trimethylene carbonates, poly(PBA- carbonates), polyfumarates, polypropylene fumarate, poly(p-dioxanone), polyhydroxyalkanoates, polyamino acids, poly-L-tyrosines, poly(beta-hydroxybutyrate), polyhydroxybutyrate-hydroxyvaleric acids, combinations thereof, or the like.

Furthermore, the filter can be formed from a ceramic material. In one aspect, the ceramic can be a biocompatible ceramic which optionally can be porous. Examples of suitable ceramic materials include hydroxylapatite, mullite, crystalline oxides, noncrystalline oxides, carbides, nitrides, suicides, borides, phosphides, sulfides, tellurides, selenides, aluminum oxide, silicon oxide, titanium oxide, zirconium oxide, alumina- zirconia, silicon carbide, titanium carbide, titanium boride, aluminum nitride, silicon nitride, ferrites, iron sulfide, and the like. Optionally, the ceramic can be provided as sinterable particles that are sintered into the shape of a filter, braid, and/or stent element.

Moreover, the filter can include a radiopaque material to increase visibility during placement. Optionally, the radiopaque material can be a layer or coating any portion of the filter. The radiopaque materials may include platinum, tungsten, silver, stainless steel, gold, tantalum, bismuth, barium sulfate, or a similar material.

It is further contemplated that the external surface and/or internal surface of the filter, braid, and/or strut element (e.g., exterior and luminal surfaces) can be coated with another material having a composition different from the primary filter material. The use of a different material to coat the surfaces can be beneficial for imparting additional properties to the filter, such as providing radiopaque characteristics, drug-reservoirs, and improved biocompatibility.

In one configuration, the external and/or internal surfaces of a filter can be coated with a biocompatible polymeric material as described herein. Such coatings can include hydrogels, hydrophilic and/or hydrophobic compounds, and polypeptides, proteins or amino acids or the like. Specific examples can include polyethylene glycols, polyvinylpyrrolidone (PVP), polyvinylalcohol (PVA), parylene, heparin, phosphorylcholine, polytetrafluorethylene (PTFE), or the like. The coatings can also be provided on the filter to facilitate the loading or delivery of beneficial agents or drugs, such as therapeutic agents, pharmaceuticals and radiation therapies. As such, the endoprosthetic material and/or holes can be filled and/or coated with a biodegradable material. Accordingly, the coating material can contain a drug or beneficial agent to improve the use of the filter. Such drugs or beneficial agents can include antithrombotics, anticoagulants, antiplatelet agents, thrombolytics, antiproliferatives, antiinflammatories, agents that inhibit hyperplasia, inhibitors of smooth muscle proliferation, antibiotics, growth factor inhibitors, or cell adhesion inhibitors, as well as antineoplastics, antimitotics, antifibrins, antioxidants, agents that promote endothelial cell recovery, antiallergic substances, radiopaque agents, viral vectors having beneficial genes, genes, siRNA, antisense compounds, oligonucleotides, cell permeation enhancers, and combinations thereof.

In one configuration, different external surfaces of a filter, such as a low stress zone less susceptible to flexing, can be coated with functional layers of an imaging compound or radiopaque material. The radiopaque material can be applied as a layer at low stress zones of the filter. Also, the radiopaque material can be encapsulated within a biocompatible or biodegradable polymer and used as a coating. For example, the suitable radiopaque material can be palladium, platinum, tungsten, silver, stainless steel, gold, tantalum, bismuth, barium sulfate, or a similar material. The radiopaque material can be applied as layers on selected surfaces of the filter using any of a variety of techniques, including cladding, bonding, adhesion, fusion, deposition or the like. V. Wall Contacts

The wall contacts of the present invention can be provided in various sizes, shapes, compositions, orientations, locations, other characteristics, or combinations thereof for different applications. Generally, the wall contacts are sized appropriately for being deployed adjacent to a lumen filter for use in a body lumen of a subject. The wall contacts are shaped to be compatible with the filter and body lumen. The composition of the wall contacts can by substantially any polymeric material; however, biodegradable wall contacts can be advantageous.

In one embodiment, the wall contact further includes a shape such as the following: a square to rectangular block cross section; a square to rectangular block cross section having a long dimension that extends from the external surface of the filter body; a square to rectangular block cross section having a convex surface coupled to the external surface of the filter body; a square to rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen or an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen. In one embodiment, each wall contact has a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject. As such, the longitudinal length of the wall contact has a dimension from about 0 mm to about 90 mm, from about 0.001 to about 25 mm, and/or about 0.1 mm to about 10 mm.

In one embodiment, the wall contact can be formed from any polymeric material disclosed herein or other similar polymers.

In one embodiment, the wall contact is formed from a biodegradable polymer selected from the group consisting of a natural polymer, synthetic polymer, polysaccharide, starch, cellulose, protein, gelatin, casein, polyesters, polyhydroxyalkanoates, lignin, shellac, natural rubber, polyalkylene esters, polylactic acids, polylactides, polyglycolic acids, polyglycolides, polyamide esters, polyvinyl esters, polyvinyl alcohols, polyanhydrides, polyesters, salts thereof, copolymers thereof, and combinations thereof. In one embodiment, the wall contact is shaped and dimensioned as a coating applied over the external surface of the filter. This can include the coating being disposed and/or extending through the apertures of the filter. Also, this can include the coating being sprayed, inkjetted, dipped, rolled, painted, or otherwise applied to the filter.

In one embodiment, the wall contact is shaped and dimensioned as a sleeve into which the filter is inserted. As such, the wall contact fits onto the filter similar to a sleeve.

In one embodiment, the wall contact can be coated with a biocompatible polymeric material as described herein. Such coatings can include hydrogels, hydrophilic and/or hydrophobic compounds, and polypeptides, proteins or amino acids or the like. Specific examples can include polyethylene glycols, polyvinylpyrrolidone (PVP), polyvinylalcohol (PVA), parylene, heparin, phosphorylcholine, polytetrafluorethylene (PTFE), or the like.

In one embodiment, the wall contact can be configured as a drug eluting wall contact. Such wall contacts are provided on the filter to facilitate the loading or delivery of beneficial agents or drugs, such as therapeutic agents, pharmaceuticals and radiation therapies.

Accordingly, the wall contact can contain a drug or beneficial agent to improve the use of the filter. Such drugs or beneficial agents can include antithrombotics, anticoagulants, antiplatelet agents, thrombolytics, antiproliferatives, antiinflammatories, agents that inhibit hyperplasia, inhibitors of smooth muscle proliferation, antibiotics, growth factor inhibitors, or cell adhesion inhibitors, as well as antineoplastics, antimitotics, antifibrins, antioxidants, agents that promote endothelial cell recovery, antiallergic substances, radiopaque agents, viral vectors having beneficial genes, genes, siRNA, antisense compounds, oligionucleotides, cell permeation enhancers, and combinations thereof. VI. Method of Making Filters

Various different manufacturing techniques are well known and may be used for fabrication of the filters, braids, strut elements, and or wall contacts of the present invention. Generally, processes for preparing endoprostheses, such as stents or filters, can be used to prepare the filters of the present invention. The filter is formed such that the braids and/or strut elements cooperate to form apertures, which function as the pores in a filter. For example, the fastener holes in the filter can be formed from a hollow tube using various techniques, such as laser cutting, EDM, milling, chemical etching, hydro- cutting, and the like. The filter can be prepared to include multiple layers or coatings deposited through a cladding process such as vapor deposition, electroplating, spraying, or similar processes. Once the generally tubular shape is formed, the tube can be shaped as described herein. Such shaping can be done before or after the forming the apertures that serve the function as a filter. Also, various other processes can be used such as those described herein.

In one embodiment, the filter can be fabricated from a sheet of suitable material, where the sheet is rolled or bent about a longitudinal axis into the desired tubular shape. Additionally, either before or after being rolled into a tube, the material can be shaped to include filter elements, fastener holes, and pores by being shaped with various techniques such as laser-cutting, milling, etching or the like. If desired, the lateral edges of the structure can be joined together, such as by welding or bonding, to form a closed tubular structure, or the lateral edges can remain unattached to form a coiled, rolled sheet or open tubular structure. Such fabrication techniques are described in more detail herein. In one embodiment, the present invention provides a method of manufacturing a filter having a wall contact for use in a body lumen of a subject. Such a method may include: forming a filter body including a plurality of filter elements interconnected together such that the filter body has a plurality of apertures disposed between and defined by the interconnected filter elements, the apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures; forming at least one fastener hole in the filter body to extend from the external surface to the internal surface; inserting at least one fastener extending through the at least one fastener hole; and coupling at least one biodegradable wall contact to the external surface of the filter body by being coupled to the at least one fastener extending through the at least one fastener hole, the wall contact having an initial thickness dimension that is substantially orthogonal to central axis of the filter body and that separates the external surface from an inner wall of the body lumen. In one embodiment, the method of manufacture may include at least one of the following: forming the wall contact to have a square to rectangular block cross section; forming the wall contact to have a square to rectangular block cross section having a long dimension that extends from the external surface of the filter body; forming the wall contact to have a square to rectangular block cross section having a convex surface coupled to the external surface of the filter body; forming the wall contact to have a square to rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; or forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen.

In one embodiment, the method of manufacture may further include forming the wall contact to have a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject.

In one embodiment, the method of manufacture may further include: forming the at least one fastener hole shaped as a keyway slot having a large portion and a narrow portion; and forming the at least one fastener to have a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot. A. Sintering

A method of making a filter can include sintering sinterable particles to provide a sintered article having the shape of the filter. The sintering can be conducted in molds that are in the shape of a general tube or in the shape of the filter. This can include molds that provide the fastener holes and/or apertures.

In one configuration, the sintered body can be obtained from a molded green body prepared by molding a mixture of sinterable particles with or without a binder into the shape of a filter or body intermediate. Sintering a molded green body that has the shape of a filter can provide a sintered body that can function as a filter with no or minimal further processing. Alternatively, after the green body has been formed in the mold and sintered into a hardened filter, the process can include shaping the sintered body with a stream of energy and/or matter in order to obtain a desired shape. This can include laser- cutting the apertures and/or forming the shape of the hourglass. Thus, sintering a green body in a mold can result in a filter that is either ready for use, or requires additional processing or finishing.

Additionally, the sintered body can be shaped into a filter as described herein. Also, the filter can be further processed after sintering and/or shaping such as by grinding, sanding, or the like to provide enhanced surface characteristics. B. Drawing Concentric Tubes

In one configuration, a multilayered filter in accordance with the present invention can be prepared by a drawing process that draws two or more distinct concentric tubes into a single tube having two or more layers. Additionally, such a drawing process can combine multiple concentric tubes into a single multilayered tube. Alternatively, the different layers can function as the different portions, such as the large diameter ends and the tapered center. The drawing process can be configured to produce junctions separating adjacent layers or bonds that bond adjacent layers. As such, the sequentially- adjacent concentric tubes can be drawn together and progressively reduced in a cross- sectional profile until the desired size and residual clamping stress is attained.

Accordingly, a metallurgical bond can be prepared with elements of each sequentially-concentric tube diffusing together and bonding to form a strong metallurgical bond. Such a metallurgical bond can be achieved by applying significant pressure and heat to the tubes. As such, a metallurgical bond can form a diffusion layer at the interface between sequentially-adjacent concentric tubes (i.e., layers). The characteristics of these diffusion layers can be controlled by the proper heat treatment cycle. In part, this is because the heat treatment, temperature, and time of processing can control the rates of transfer of the diffusing elements that produce the diffusion layers. Also, the pressure at the interface between layers can be developed to result in the residual radial clamping stress in the tube after drawing.

In one example of this process, an outer tube of nitinol, a middle tube of tantalum, and an inner tube of nitinol can be arranged to form the composite structure. The multilayered material can be produced to result in bonding between the layers to achieve a residual clamping stress of at least about 90 p.s.i. Accordingly, the annealing process can be performed within a limited range of time and temperatures. For example, the lower limit can be at least about 1550⁰F for at least six minutes, and the upper limit can be less than about 1850⁰F for less than 15 minutes.

In another configuration, a metallic interleaf layer can be placed between separate tubes to bond the tubes together and form a multilayered material. The multiple tubes separated by the metallic interleaf layer can be drawn together and progressively reduced until the desired cross- sectional profile and residual clamping stress is attained, as described herein. The drawn tubes can be heat-treated to form a diffusion bond between the separate layers. As such, the metallic interleaf layer can enhance the diffusion rate or type of diffusing atoms that are transported across a diffusion region between one layer and the interleaf layer.

In one configuration, a multilayered sheet can be prepared to have separate layers of different materials or the same material. For example, the multilayered sheet can have a top layer of nitinol, a middle layer of tantalum, and a bottom layer of Nitinol. The sheet can be prepared by metallurgically bonding the layers prior to a deep drawing process. During the deep drawing process, the sheet can be placed over a die and forced into the die, such as by a punch or the like. A tube having a closed end and a defined wall thickness can be formed in the die. This process can be repeated using a series of dies that have progressively decreasing diameters until a multilayered tube is formed having the desired diameter and wall thickness. For certain material combinations, intermediate heat treatments can be performed between the progressive drawing operations to form a multilayered material that may be resistant to delaminating. Once a multilayered tube of desired thickness and dimensions has been formed, the closed end and the curved edges can be cut off. Then, the tube can be heat treated, as described above, until proper inter- metallic bonds are formed between the layers. C. Shaping

Accordingly, a filter material can be shaped by various methods as described in more detail below. This can include shaping the apertures and fastener holes into the filter body. Such shaping techniques can utilize streams of energy and/or streams of matter in order to impart shapes into the filter material. The streams of energy may include photons, electromagnetic radiation, atomic, and sub-atomic materials, as described herein. On the other hand, the streams of matter are considered to include materials larger than atomic scale particles, and can be microscopic or macroscopic in size. In any event, the shaping can be designed to direct a stream of energy or a stream of matter at the filter material to form an endoprosthetic element and/or holes therein.

In one configuration, a stream of energy can cut, shape, and/or form a tube into a filter by generating heat at the site where the stream intersects the material. The thermal interaction can elevate the local temperature to a point, which can cut, melt, shape, and/or vaporize portions of the filter material from the rest of the material. Accordingly, one configuration of the stream-cutting apparatus can operate and shape the filter material by thermal interactions. As such, any of the thermal processes described herein can be used for thermal-cutting. For example, such thermal interactions can arise from laser beam treatment, laser beam machining, electron beam machining, electrical discharge machining, ion beam machining, and plasma beam machining. In one configuration, by knowing the thermal properties of the filter material, precise energy requirements can be calculated so that the thermal beam provides the appropriate or minimum energy for melting and/or vaporizing the material without significantly melting undesirable portions of the material. For example, laser beams are a common form of a stream of energy that can be used to shape the filter material. Additionally, there are instances where a laser is preferred over all other cutting techniques because of the nature of the resulting filter as well as the characteristics of the filter material.

In one configuration, a filter may be manufactured as described herein using a femtosecond laser. A femtosecond laser may be desirable in producing an endoprosthesis in accordance with the multilayered composite structure of the present invention because it produces a smaller heat influence zone (HIZ) or heat affected zone (HAZ) compared to other lasers, or it can substantially eliminate the HIZ or HAZ. In comparison, cutting a filter using various methods can result in the tubular material being melted away, and thereby forming the pattern in the tubular member. Such melting can result in embrittlement of some materials due to oxygen uptake into the HIZ.

In one configuration, electrical discharge machining is used to shape filter material and/or form holes in the material as desired. As such, electrical discharge machining can be capable of cutting all types of conductive materials such as exotic metal including titanium, hastaloy, kovar, hard tool steels, carbides, and the like. In electrical discharge, the main interaction between the stream of energy and the filter material is thermal, where heat is generated by producing electrical discharges. This can lead to the filter material being removed by melting and evaporation. Some examples of electrical discharge machining include wire electron discharge machining, CNC-controlled electrical discharge machining, sinker electrical discharge machining, small hole discharge machining, and the like.

In another configuration, a charged particle beam can be used for shaping the filter material, wherein electron beams and ion beams exemplify charged particle beams. A charged particle beam is a group of electrically-charged particles that have approximately the same kinetic energy and move in approximately the same direction. Usually, the kinetic energies are much higher than the thermal energies of similar particles at ordinary temperatures. The high kinetic energy and the directionality of these charged beams can be useful for cutting and shaping of the green bodies, as described herein. Additionally, there are some instances where electron beams or ion beams are preferred over other cutting techniques.

In one configuration, a stream of chemical matter can be used in order to shape or form holes in the filter material. Chemical-jet milling, for example, provides selective and controlled material removal by jet and chemical action. As such, the process is similar to water-jet cutting, which is described in more detail below. In any event, chemical-jet milling can be useful for shaping various types of filter materials, which provides intricate shaping capabilities.

In another configuration, electrochemical shaping can be based on a controlled electrochemical dissolution process similar to chemical-jet milling a filter material. As such, the filter material can be attached to an electrical source in order to allow an electrical current to assist in the shaping.

In one configuration, hydro-cutting or water-jet cutting can be used to shape a filter material. Hydro-cutting is a water-jet technology that uses the high force and high pressure of a stream of water directed at the filter material in order to cut and shape the material as desired. Hydro-cutting can be preferred over some of the other stream-cutting technologies because it can be free of heat, flame, and chemical reactions, and can provide a precise cold shaping technique. Also, heated water with or without being doped with reactive chemicals can also be used. Hydro-cutting is particularly suitable for polymeric filters, but can be used for metal materials when combined with abrasive particles, as described below.

Additionally, hydro-cutting can be enhanced by the introduction of particulate materials into the water feed line. As such, some hydro-cutting techniques utilize garnet or other rigid and strong materials in order to apply an abrasive cutting force along with the force applied by the water itself. Also, the hydro-cutting process in the present invention can be used with or without inclusion of such abrasives.

Additionally, one of the benefits of hydro-cutting is the ability to reutilize and recycle the spent water-jet material. As such, the filter material can be easily separated from the spent water, thereby enabling the recycling and reuse of the water during the hydro-cutting process. In one configuration, sandblasting, which fits into the regime of stream of matter cutting, can be used to shape a filter material by projecting a high energy stream of sand particles at the material. Sandblasting cuts materials in a manner similar to hydro-cutting, especially when the water-jet is doped with abrasive particulates. Additionally, various other particulate streams other than sand can be used in the stream-cutting techniques and machinery.

D. Heat Setting

In general, a filter may be manufactured into the free recovery shape through heat setting a superelastic material. If the superelastic filter is required for a particular application, such as inside of a superficial femoral artery, the large end of the filter may need to be as large as about 10 millimeters. Increasing the diameter of the large end of the filter and/or forming the conical or funnel shape can be a gradual process with individual steps often being expansions of only 1 millimeter. This allows the diameter of the large end portion and the enlargement of the conical portion to be gradually increased in size from the center point or the center conduit of the filter. The number of steps that are repeated can be up to and over 10 steps. Therefore, in the case of having a superelastic nitinol hollow tube with an inner diameter of 1.3 millimeters, after about 8 steps, the diameter of the large end portions may be around 10 millimeters, which is typically sufficient for most intraluminal endoprosthestic applications within the human body. The beginning diameter and the final diameter of the large end portions may be smaller or larger depending upon the desired final diameter that a filter needs to be for a particular application.

When the filter is configured to have the final diameter necessary (e.g., diameter of large end portion) for its particular application, the filter may then be heated according to the method of the present invention in order to provide the filter shape.

In one embodiment, a nickel titanium or nitinol filter can be heat set. Heat setting is a process whereby the nitinol, or other superelastic material, is heated to a temperature far above its austenitic finish temperature in a desired shape, (e.g., large end portions, tapered central portion, cones, filters, hourglass and/or the like), followed by water quenching. A filter may be deformed at the heat set temperature into a new shape, such as being transformed from a cylindrical shape to the filter shape. When the filter is cooled so it is in the martensitic form, the filter may be deformed into the delivery configuration. When the deformed, martensitic filter is introduced into a body lumen, for example, the temperature of the filter rises to (and above) the austenitic finish temperature and the filter will then reform to the heat set filter shape.

The temperature and the time of heating of the filter depend upon the composition of the superelastic metal and the particular application of filter. For example, a nitinol superelastic metal alloy having a composition of 49% nickel and 51% titanium can have different characteristics than a nitinol superelastic metal alloy having a binary composition of nickel and titanium. Using a standard superelastic nitinol (55.3-56.3 wt. % Ni), a temperature of about 900 degrees Celsius for about 30 seconds or more is preferable to configure the filter into the hourglass shape. A useable range of temperatures for standard superelastic nitinol metals is from about 400 to about 600 degrees Celsius for greater than about 30 seconds. Temperature ranges and times of heat treatment also change when strengthening elements such as Cr are added. E. Forming Wall Contact

Generally, the wall contacts can be prepared by any process for preparing polymeric members. Examples of such a process include the following: shaping a block of the polymer into the shape of the wall contact; molding the wall contact from the polymer; injection molding the wall contact; stamping the wall contact from a polymeric sheet; dip coating the polymer onto the filter to form a wall contact; and other similar processes for preparing polymeric members. In one embodiment, the method of manufacture may include at least one of the following: forming the wall contact to have a square to rectangular block cross section; forming the wall contact to have a square to rectangular block cross section having a long dimension that extends from the external surface of the filter body; forming the wall contact to have a square to rectangular block cross section having a convex surface coupled to the external surface of the filter body; forming the wall contact to have a square to rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; or forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen. F. Coupling Wall Contact With Filter

The wall contact can be permanently or removably coupled to the filter. There are a variety of processes for attaching a first member to a second member of a medical device. This can include the use of fasteners, adhesives, coatings, couplings and the like. In the instance of a wall contact in the form of a coating, the coating can be applied to the filter. Usually, coatings are not removable except when the biodegradable polymer is fully depleted. As such, the coating can be formed onto the filter by being sprayed, inkjetted, dipped, rolled, painted, or otherwise applied to the filter. In the instance of a wall contact in the form of a sleeve, the sleeve is preformed and the filter is inserted therein. The sleeve can be form-fitted to the filter and/or adhesives can be used to secure the sleeve to the filter.

In the instance the wall contact is a polymeric member, the fasteners of the present invention can be used to removably or permanently couple the wall contact to the filter. The fastener and wall contact can form a fastener system substantially similar to those used in the medical arts to attach one medical component to another medical component. For example, the fastener system can include the wall contact having a bolt-like protrusion extending through the fastener hold of the filter with a nut securing the wall contact to the filter by being fitted onto the bolt-like protrusion. In another example, the fastener is a nail-like structure integrated with the wall contact or formed therewith. In yet another example, the fastener is a screw that fits through the fastener hole and into the wall contact, where the screw head is larger than at least a portion of the fastener hole. In still yet another example, the wall contact includes a recess, such as a threaded recess, to receive the fastener.

Additionally, the wall contact can be removably coupled to the filter by forming the filter to have at least one keyway slot shape and to form the fastener to have a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot. As such, the head portion can be inserted through the large portion of the keyway slot until the stem is disposed therein. The stem is then slid into the narrow portion of the keyway slot such that the head portion is disposed on the internal surface of the filter. G. Additional Processing

An additional step of passivation can be performed during the manufacturing stage of the filter in order to form a homogeneous oxide layer for corrosion-resistance. The passivation process may be performed prior to installation of radiopaque markers in accordance with the present invention or it may be performed after installation of the radiopaque markers. Alternatively, multiple passivation processes may be performed, once prior to application of the markers, and again after insertion of the markers. As originally shaped and/or fabricated, the filter can correspond to its delivery configuration, to a deployed configuration, or to a configuration therebetween. The filter can be fabricated with a configuration at least slightly larger than the delivery configuration. In this manner, the filter can be crimped or otherwise compressed into its delivery configuration in a corresponding delivery device. In another configuration, the filter can be originally fabricated from a tube having a diameter corresponding to the deployed configuration. The filter can be designed to match the target vessel in which the filter is to be deployed. For example, a stent can be provided with an outer diameter in the deployed configuration ranging from about 1 mm for neurological vessels to about 25 mm for the aorta. Similarly, a stent can be provided with a length ranging from about 9 mm to about 200 mm. Variations of these dimensions will be understood in the art based upon the intended application or indication for the filter.

The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.

Claims

1. A filter for use in a body lumen of a subject, the filter comprising: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, said apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures; and at least one biodegradable wall contact coupled to at least one of the filter elements on the external surface of the filter body, said wall contact having an initial thickness dimension that is substantially orthogonal to central axis of the filter body and that separates the external surface from an inner wall of the body lumen.

2. The filter as in claim 1, where the filter body includes at least one of the following: a substantially funnel shape with a conduit having a larger end opposite of a smaller end, said smaller end being dimensioned to inhibit a thrombus of a selected size from passing therethrough; a substantially cone shape with a cavity having a larger end opposite of an apex to inhibit a thrombus of a selected size from passing therethrough; or a substantially hourglass shape with a conduit having a narrow median portion being dimensioned to inhibit a thrombus of a selected size from passing therethrough.

3. The filter as in claim 2, said at least one wall contact further comprising at least one of the following: a rectangular block cross section; a rectangular block cross section having a long dimension that extends from the external surface of the filter body; a rectangular block cross section having a convex surface coupled to the external surface of the filter body; a rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; or an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen.

4. The filter as in claim 3, wherein the at least one wall contact has a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject.

5. The filter as in claim 4, wherein the longitudinal length of the at least one wall contact has a dimension from about 0 mm to about 90 mm.

6. The filter as in claim 4, wherein the at least one wall contact is dimensioned to inhibit endothelial cell ingrowth into the apertures.

7. The filter as in claim 1, further comprising at least one of the following: the at least one wall contact being coated onto the external surface to extend into at least a portion of the plurality of apertures; at least one filter element defining a hole with a portion of the wall contact extending therethrough; at least one filter element defining a hole with a fastener extending therethrough and coupling with the at least one wall contact; at least one filter element defining a hole shaped as a keyway slot and a portion of the wall contact extending therethrough; at least one filter element defining a hole shaped as a keyway slot with a fastener extending therethrough and coupling with the at least one wall contact; at least one filter element defining a hole shaped as a keyway slot having a large portion and a narrow portion and a portion of the wall contact extending therethrough, said portion of the wall contact having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot; or at least one filter element defining a hole shaped as a keyway slot having a large portion and a narrow portion with a fastener extending therethrough and coupling with the at least one wall contact, said fastener having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

8. The filter as in claim 1, further comprising at least one fastener coupling the at least one wall contact to the external surface of the filter body.

9. The filter as in claim 1, wherein the biodegradable polymer is selected from the group consisting of a natural polymer, synthetic polymer, polysaccharide, starch, cellulose, protein, gelatin, casein, polyesters, polyhydroxyalkanoates, lignin, shellac, natural rubber, polyalkylene esters, polylactic acids, polylactides, polyglycolic acids, polyglycolides, polyamide esters, polyvinyl esters, polyvinyl alcohols, polyanhydrides, polyesters, salts thereof, copolymers thereof, and combinations thereof.

10. The filter as in claim 1, further comprising: the filter body having an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen and is dimensioned to inhibit endothelial cell ingrowth into the apertures; and at least one filter element defining a hole shaped as a keyway slot having a large portion and a narrow portion with a fastener extending therethrough and coupling with the at least one wall contact, said fastener having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

11. A filter for use in a body lumen of a subject, the filter comprising: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, said apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures; at least one filter element defining at least one fastener hole extending from the external surface to the internal surface; at least one fastener extending through the at least one fastener hole; and at least one biodegradable wall contact removably coupled to the at least one filter element on the external surface of the filter body by being coupled to the at least one fastener extending through the at least one fastener hole, said wall contact having an initial thickness dimension that is substantially orthogonal to central axis of the filter body and that separates the external surface from an inner wall of the body lumen.

12. The filter as in claim 11, where the filter body has at least one of the following: a substantially funnel shape with a conduit having a larger end opposite of a smaller end, said smaller end being dimensioned to inhibit a thrombus of a selected size from passing therethrough; a substantially cone shape with a cavity having a larger end opposite of an apex to inhibit a thrombus of a selected size from passing therethrough; or a substantially hourglass shape with a conduit having a narrow median portion being dimensioned to inhibit a thrombus of a selected size from passing therethrough.

13. The filter as in claim 12, said at least one wall contact further comprising at least one of the following: a rectangular block cross section; a rectangular block cross section having a long dimension that extends from the external surface of the filter body; a rectangular block cross section having a convex surface coupled to the external surface of the filter body; a rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; or an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen.

14. The filter as in claim 13, wherein the at least one wall contact has a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject.

15. The filter as in claim 14, wherein the longitudinal length of the at least one wall contact has a dimension from about 0 mm to about 90 mm.

16. The filter as in claim 14, wherein the at least one wall contact is dimensioned to inhibit endothelial cell ingrowth into the apertures.

17. The filter as in claim 11, further comprising at least one of the following: the at least one fastener hole being shaped as a keyway slot; the at least one fastener hole being shaped as a keyway slot with the at least one fastener extending therethrough and coupling with the at least one wall contact; the at least one fastener hole being shaped as a keyway slot having a large portion and a narrow portion with the at least one fastener extending therethrough and coupling with the at least one wall contact, said fastener having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

18. The filter as in claim 11, wherein the at least one fastener is at least one of the following: integrated with the at least one wall contact; removably coupled with the at least one wall contact; or a portion of the at least one wall contact.

19. The filter as in claim 11, wherein the biodegradable polymer is selected from the group consisting of a natural polymer, synthetic polymer, polysaccharide, starch, cellulose, protein, gelatin, casein, polyesters, polyhydroxyalkanoates, lignin, shellac, natural rubber, polyalkylene esters, polylactic acids, polylactides, polyglycolic acids, polyglycolides, polyamide esters, polyvinyl esters, polyvinyl alcohols, polyanhydrides, polyesters, salts thereof, copolymers thereof, and combinations thereof.

20. The filter as in claim 11, further comprising: the filter body having an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen and is dimensioned to inhibit endothelial cell ingrowth into the apertures; and the at least one fastener hole shaped as a key way slot having a large portion and a narrow portion with the at least one fastener extending therethrough and coupling with the at least one wall contact, said fastener having a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

21. A method of manufacturing a filter for use in a body lumen of a subject, the method comprising: forming a filter body comprised of a plurality of filter elements interconnected together such that the filter body has a plurality of apertures disposed between and defined by the interconnected filter elements, said apertures extending from an external surface to an internal surface of the filter body and being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures; forming at least one fastener hole in the filter body to extend from the external surface to the internal surface; inserting at least one fastener extending through the at least one fastener hole; and coupling at least one biodegradable wall contact to the external surface of the filter body by being coupled to the at least one fastener extending through the at least one fastener hole, said wall contact having an initial thickness dimension that is substantially orthogonal to a central axis of the filter body and that separates the external surface from an inner wall of the body lumen.

22. The method as in claim 21, further comprising at least one of the following: forming the wall contact to have a rectangular block cross section; forming the wall contact to have a rectangular block cross section having a long dimension that extends from the external surface of the filter body; forming the wall contact to have a rectangular block cross section having a convex surface coupled to the external surface of the filter body; forming the wall contact to have a rectangular block cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and an opposite convex surface configured to conform with the inner wall of the body lumen; or forming the wall contact to have an arc-shaped cross section having a concave surface coupled to the external surface of the filter body and extending around at least 1/4 of a circumference of the external surface of the filter body, and having an opposite convex surface configured to conform with the inner wall of the body lumen.

23. The method as in claim 22, further comprising forming the wall contact to have a longitudinal length dimensioned to inhibit the filter from migrating within the body lumen of the subject.

24. The method as in claim 21, further comprising: forming the at least one fastener hole shaped as a keyway slot having a large portion and a narrow portion; and forming the at least one fastener to have a stem that fits through the narrow portion of the keyway slot and a head portion that fits through the large portion and that is larger than the narrow portion of the keyway slot.

25. The method as in claim 24, wherein the biodegradable polymer is selected from the group consisting of a natural polymer, synthetic polymer, polysaccharide, starch, cellulose, protein, gelatin, casein, polyesters, polyhydroxyalkanoates, lignin, shellac, natural rubber, polyalkylene esters, polylactic acids, polylactides, polyglycolic acids, polyglycolides, polyamide esters, polyvinyl esters, polyvinyl alcohols, polyanhydrides, polyesters, salts thereof, copolymers thereof, and combinations thereof.

26. A filter for use in a body lumen of a subject, the filter comprising: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, said apertures being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures, said filter body comprising: a first funnel having a first funnel-shaped body defining a first conduit having a first larger end fluidly coupled to and opposite of a first smaller end, said first funnel-shaped body having a plurality of first apertures defined by the interconnected filter elements; and a second funnel having a second funnel-shaped body defining a second conduit having a second larger end fluidly coupled to and opposite of a second smaller end, said second funnel-shaped body having a plurality of second apertures defined by the interconnected filter elements, said second smaller end of the second funnel being fluidly coupled to the first smaller end of the first funnel, said first smaller end and second smaller end being dimensioned to inhibit a thrombus of a selected size from passing therethrough.

27. The filter as in claim 26, wherein the filter body is configured such that the first larger end of the first funnel and the second larger end of the second funnel have a reduced dimension when tensile longitudinal forces are applied to the filter body.

28. The filter as in claim 27, wherein the filter body is configured such that the first larger end of the first funnel and the second larger end of the second funnel have an enlarged dimension when compressive longitudinal forces are applied to the filter body or tensile forces are released from the filter body.

29. The filter as in claim 28, said filter body further comprising at least one of the following: a first tube having a first tube- shaped body defining a first tube conduit and having a first end fluidly coupled to the first larger end of the first funnel- shaped body, said first tube having a first length; or a second tube having a second tube-shaped body defining a second tube conduit and having a second end fluidly coupled to the second larger end of the second funnel-shaped body, said second tube having a second length.

30. The filter as in claim 29, wherein at least one of the following: the first length of the first tube is dimensioned to inhibit the filter from migrating within the body lumen of the subject; or the second length of the second tube is dimensioned to inhibit the filter from migrating within the body lumen of the subject.

31. The filter as in claim 30, wherein at least one of the first length or second length has a dimension from about 0 mm to about 50 mm.

32. The filter as in claim 28, wherein at least one of the first funnel or second funnel is shaped to trap the thrombus of the selected size within the respective conduit at a central axial position, and at least one of the first apertures or second apertures are dimensioned to inhibit the thrombus of the selected size from passing therethrough and being dimensioned to allow blood components smaller than the selected size to pass therethrough.

33. The filter as in claim 28, wherein the filter body has sufficient rigidity to reconfigure the body lumen from an oblong-shaped cross section to a circular- shaped cross section.

34. The filter as in claim 28, wherein the interconnected filter elements are formed from laser shaping the filter body.

35. The filter as in claim 28, wherein the interconnected filter elements are formed from braids.

36. A filter for use in a body lumen of a subject, the filter comprising: a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, said apertures being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures, said filter body comprising: a first funnel having a first funnel-shaped body defining a first conduit having a first larger end fluidly coupled to and opposite of a first smaller end, said first funnel-shaped body having a plurality of first apertures defined by the interconnected filter elements; a second funnel having a second funnel-shaped body defining a second conduit having a second larger end fluidly coupled to and opposite of a second smaller end, said second funnel-shaped body having a plurality of second apertures defined by the interconnected filter elements; and a median portion having a median body defining a median conduit having a first end coupled to the first smaller end of the first funnel and having a second end coupled to the second smaller end of the second funnel, said median conduit being dimensioned to inhibit a thrombus of a selected size from passing through the median conduit.

37. The filter as in claim 36, wherein the filter body is configured such that the first larger end of the first funnel and the second larger end of the second funnel have a reduced dimension when tensile longitudinal forces are applied to the filter body.

38. The filter as in claim 37, wherein the filter body is configured such that the first larger end of the first funnel and the second larger end of the second funnel have an enlarged dimension when compressive longitudinal forces are applied to the filter body or tensile forces are released from the filter body.

39. The filter as in claim 38, said filter body further comprising at least one of the following: a first tube having a first tube- shaped body defining a first tube conduit and having a first end fluidly coupled to the first larger end of the first funnel- shaped body, said first tube having a first length; or a second tube having a second tube-shaped body defining a second tube conduit and having a second end fluidly coupled to the second larger end of the second funnel-shaped body, said second tube having a second length.

40. The filter as in claim 39, wherein at least one of the following: the first length of the first tube is dimensioned to inhibit the filter from migrating within the body lumen of the subject; or the second length of the second tube is dimensioned to inhibit the filter from migrating within the body lumen of the subject.

41. The filter as in claim 40, wherein at least one of the first length or second length has a dimension from about 0 mm to about 50 mm.

42. The filter as in claim 38, wherein at least one of the first funnel or second funnel is shaped to trap the thrombus of the selected size within the respective conduit at a central axial position, and at least one of the first apertures or second apertures are dimensioned to inhibit the thrombus of the selected size from passing therethrough and being dimensioned to allow blood components smaller than the selected size to pass therethrough.

43. The filter as in claim 38, wherein the filter body has sufficient rigidity to reconfigure the body lumen from an oblong-shaped cross section to a circular- shaped cross section.

44. The filter as in claim 38, wherein the interconnected filter elements are formed from laser shaping the filter body.

45. The filter as in claim 38, wherein the interconnected filter elements are formed from braids.

46. A method of utilizing a filter in a body lumen of a subject, the method comprising: providing a luminal filter having a plurality of filter elements interconnected to form a filter body having a plurality of apertures disposed between and defined by the interconnected filter elements, said apertures being dimensioned to inhibit a thrombus of a selected size from passing through the apertures and being dimensioned to allow blood components smaller than the selected size to pass through the apertures, said filter body comprising: a first funnel having a first funnel-shaped body defining a first conduit having a first larger end fluidly coupled to and opposite of a first smaller end, said first funnel-shaped body having a plurality of first apertures defined by the interconnected filter elements; and a second funnel having a second funnel-shaped body defining a second conduit having a second larger end fluidly coupled to and opposite of a second smaller end, said second funnel-shaped body having a plurality of second apertures defined by the interconnected filter elements; said second smaller end of the second funnel being fluidly coupled to the first smaller end of the first funnel, said first smaller end and second smaller end being dimensioned to inhibit a thrombus of a selected size from passing therethrough; longitudinally elongating the filter body such that the first larger end of the first funnel and the second larger end of the second funnel have a reduced dimension; delivering the elongated filter body to a desired deployment site within the body lumen of the subject; and longitudinally shortening the filter body such that the first larger end of the first funnel and the second larger end of the second funnel each have an enlarged dimension that applied radial forces to an inner wall of the body lumen.

47. The method as in claim 46, said filter body further comprising at least one of the following: a first tube having a first tube- shaped body defining a first tube conduit and having a first end fluidly coupled to the first larger end of the first funnel- shaped body, said first tube having a first length; a second tube having a second tube-shaped body defining a second tube conduit and having a second end fluidly coupled to the second larger end of the second funnel-shaped body, said second tube having a second length; or a median portion having a median body defining a median conduit having a first end coupled to the first smaller end of the first funnel and having a second end coupled to the second smaller end of the second funnel, said median conduit being dimensioned to inhibit a thrombus of a selected size from passing through the median conduit.

48. The method as in claim 47, wherein at least one of the following: the first length of the first tube is dimensioned to inhibit the filter from migrating within the body lumen of the subject; or the second length of the second tube is dimensioned to inhibit the filter from migrating within the body lumen of the subject.

49. The method as in claim 46, further comprising longitudinally elongating the filter body such that the first larger end of the first funnel and the second larger end of the second funnel have a reduced dimension with a cross section that is smaller than the body lumen; and retrieving the elongated filter body from the desired deployment site within the body lumen of the subject.

50. The method as in claim 49, wherein at least one of the delivering or retrieving is performed with a catheter.