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A thrombus treatment device includes a support wire, a body frame portion that is disposed about an axis defined by the support wire, one or more tethers that each have a first end and a second end, and a filter element extending from the body frame portion. Each of the one or more tethers is attach

A thrombus treatment device includes a support wire, a body frame portion that is disposed about an axis defined by the support wire, one or more tethers that each have a first end and a second end, and a filter element extending from the body frame portion. Each of the one or more tethers is attached at its first end to the body frame portion, and at its second end to a collar that couples the second end of each of the multiple tethers to the support wire. When the collar is positioned substantially within a region interior of the body frame portion, a rotational actuation of the support wire causes a swiveling motion of the one or more tethers.

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1. A thrombus treatment device, comprising: a support tube defining a longitudinal axis;a body frame portion that is disposed about the longitudinal axis defined by the support tube, the body frame portion including a proximal end and a distal end;a filter portion that extends from the distal end of

1. A thrombus treatment device, comprising: a support tube defining a longitudinal axis;a body frame portion that is disposed about the longitudinal axis defined by the support tube, the body frame portion including a proximal end and a distal end;a filter portion that extends from the distal end of the body frame portion; andmultiple tethers each having a first end and a second end, wherein the first end of each of the multiple tethers extends out a proximal end of the support tube, the tethers extending through a lumen of the support tube and out a distal end of the support tube and engaging the body frame portion near the distal end of the body frame portion and extending to the proximal end of the body frame portion, the second end of each of the multiple tethers being attached to the body frame portion near the proximal end of the body frame portion, wherein each tether of the multiple tethers forms a loop around the body frame portion near the proximal end of the body frame portion. 2. The thrombus treatment device of claim 1, wherein a longitudinal length of the body frame portion is at least three times as long as an outer diameter of the body frame portion. 3. The thrombus treatment device of claim 1, wherein a longitudinal length of the body frame portion is at least four times as long as an outer diameter of the body frame portion. 4. The thrombus treatment device of claim 1, wherein a longitudinal length of the body frame portion is at least five times as long as an outer diameter of the body frame portion. 5. The thrombus treatment device of claim 1, wherein a longitudinal length of the filter portion is less than or equal to one-half of the longitudinal length of the body frame portion. 6. The thrombus treatment device of claim 1, wherein one or more tethers are comprised of nitinol. 7. The thrombus treatment device of claim 1, wherein one or more tethers are comprised of a polymeric material. 8. The thrombus treatment device of claim 1, wherein the tethers extend from the distal end of the support tube near a central collar that is coupled thereto. 9. The thrombus treatment device of claim 1, wherein the filter portion does not substantially overlap the body frame portion. 10. The thrombus treatment device of claim 1, wherein the body frame portion defines a plurality of open-faced cells arranged in at least three rows along a longitudinal length of the body frame portion, and wherein the filter portion overlaps the body frame portion by up to one row of the at least three rows and does not overlap a remaining body frame portion. 11. The thrombus treatment device of claim 10, wherein the body frame portion defines from three to ten rows of open-faced cells along the longitudinal length of the body frame portion. 12. The thrombus treatment device of claim 1, wherein the filter portion overlaps 20% or less of a longitudinal length of the body frame portion. 13. The thrombus treatment device of claim 1, wherein a proximally directed force applied to the first end of each of the multiple tethers causes the distal end of the body frame portion and the proximal end of the body frame portion to collapse radially toward the longitudinal axis defined by the support tube. 14. A thrombus treatment device, comprising: a support tube defining a longitudinal axis;a body frame portion that is disposed about the longitudinal axis defined by the support tube, the body frame portion including a proximal end and a distal end;a filter portion that extends from the distal end of the body frame portion; andmultiple tethers each having a first end and a second end, wherein the first end of each of the multiple tethers extends out a proximal end of the support tube, the tethers extending through a lumen of the support tube and out a distal end of the support tube and engaging the body frame portion near the distal end of the body frame portion and extending to the proximal end of the body frame portion, the second end of each of the multiple tethers being attached to the body frame portion near the proximal end of the body frame portion, wherein the multiple tethers collectively form a loop around the body frame portion near the proximal end of the body frame portion. 15. The thrombus treatment device of claim 14, wherein a proximally directed force applied to the first end of each of the multiple tethers causes the distal end of the body frame portion and the proximal end of the body frame portion to collapse radially toward the longitudinal axis defined by the support tube. 16. The thrombus treatment device of claim 14, wherein a longitudinal length of the body frame portion is at least three times as long as an outer diameter of the body frame portion. 17. The thrombus treatment device of claim 14, wherein a longitudinal length of the body frame portion is at least four times as long as an outer diameter of the body frame portion. 18. The thrombus treatment device of claim 14, wherein a longitudinal length of the body frame portion is at least five times as long as an outer diameter of the body frame portion. 19. The thrombus treatment device of claim 14, wherein a longitudinal length of the filter portion is less than or equal to one-half of the longitudinal length of the body frame portion. 20. The thrombus treatment device of claim 14, wherein one or more tethers are comprised of nitinol. 21. The thrombus treatment device of claim 14, wherein one or more tethers are comprised of a polymeric material. 22. The thrombus treatment device of claim 14, wherein the tethers extend from the distal end of the support tube near a central collar that is coupled thereto. 23. The thrombus treatment device of claim 14, wherein the filter portion does not substantially overlap the body frame portion. 24. The thrombus treatment device of claim 14, wherein the body frame portion defines a plurality of open-faced cells arranged in at least three rows along a longitudinal length of the body frame portion, and wherein the filter portion overlaps the body frame portion by up to one row of the at least three rows and does not overlap a remaining body frame portion. 25. The thrombus treatment device of claim 24, wherein the body frame portion defines from three to ten rows of open-faced cells along the longitudinal length of the body frame portion. 26. The thrombus treatment device of claim 14, wherein the filter portion overlaps 20% or less of a longitudinal length of the body frame portion.