Flexible embolic double filter

1. An intraluminal filtration device for embolic protection comprising:

a device body defining a longitudinal axis and having formed therein a central lumen extending longitudinally between a proximal body end and a distal body end;

a coarse filter located at the proximal body end and positioned to block larger-size particles from passing between the central lumen and a vessel lumen in a patient vessel receiving the filtration device;

a fine filter located at the distal body end to form a porous end wall of the central lumen that is intersected by the longitudinal axis and position to block smaller-size particles from passing between the central lumen and the vessel lumen;

the device body further including a body wall formed of an organic gel to include an inner surface defining an inner cylinder and an outer surface defining an outer cylinder extending circumferentially around and along the longitudinal axis from the proximal body end to the distal body end; and

wherein the body wall is radially compliant, and further comprising at least one tensile-strengthening member attached to the device body and extending between the proximal and distal body ends such that the device body is axially incompliant.

2. The device of claim 1 wherein the fine filter includes a textile and is shaped and attached to the body wall such that the fine filter radially deforms during compliance of the body wall with the patient vessel during dilation and constriction thereof.

3. The device of claim 2 wherein the fine filter has a dome shape and projects axially outward from the distal body end.

4. The device of claim 2 wherein the coarse filter includes a plurality of perforations defined by the device body.

5. The device of claim 1 wherein the at least one tensile-strengthening member includes one of a plurality of non-metallic fibers.

6. The device of claim 1 further comprising a skeleton attached to the device body and formed of a second material different from the organic gel.

7. The device of claim 6 wherein the device body is formed throughout of the organic gel, and the organic gel has a Shore 00 hardness of about 30 or less.

8. The device of claim 7 wherein the skeleton includes an endoskeleton and the second material is a non-biodegradable organic material.

9. The device of claim 7 further comprising a retrieval hook attached to the skeleton.

10. A method for embolic protection with an intraluminal filtration device that includes a device body defining a longitudinal axis and having formed therein a central lumen extending longitudinally between a proximal body end and a distal body end; a coarse filter located at the proximal body end and positioned to block larger-size particles from passing between the central lumen and a vessel lumen in a patient vessel receiving the filtration device; a fine filter located at the distal body end to form a porous end wall of the central lumen that is intersected by the longitudinal axis and positioned to block smaller-size particles from passing between the central lumen and the vessel lumen; and the device body further including a body wall formed of an organic gel to include an inner surface defining an inner cylinder and an outer surface defining an outer cylinder extending circumferentially around and along the longitudinal axis from the proximal body end to the distal body end, wherein the body wall is radially compliant, and further comprising at least one tensile-strengthening member attached to the device body and extending between the proximal and distal body ends such that the device body is axially incompliant, the method comprising the steps of:

positioning the filtration device within the vessel in the patient such that the coarse filter and the fine filter of the filtration device are positioned at upstream and downstream locations, respectively, within the patient vessel;

placing the body wall of the filtration device formed of the organic gel in contact with the patient vessel; and

forming a fluid seal between the cylindrical wall and the patient vessel via the contact, such that fluid flowing through the patient vessel passes through the central lumen formed by the cylindrical wall and is filtered via each of the coarse and fine filters.

11. The method of claim 10 further comprising a step of relieving radial compressive force on the filtration device during the placement of the cylindrical wall, such that an elastically deformed skeleton of the filtration device responsively urges the cylindrical wall into contact with the patient vessel.

12. The method of claim 11 wherein the skeleton is formed of a non-biodegradable organic material.

13. The method of claim 11 further comprising a step of retaining the filtration device within the patient vessel once positioned, via retention elements protruding out from the cylindrical wall.

14. The method of claim 10 wherein the filtering includes filtering larger-size particles from the fluid via perforations forming the coarse filter in the device body of the filtration device.

15. The method of claim 14 wherein the device body is formed of the organic gel throughout.

16. The method of claim 14 wherein the filtering includes filtering the smaller-size particles via a textile attached to the device body and forming the fine filter.

17. The method of claim 10 further comprising a step of cleaning the filtration device of accumulated embolic particles.