IP Library Granted Patent US 7,485,122
Granted Patent B2
US 7,485,122 · App. 10/185,671 · Granted Feb 3, 2009

Integrated anchor coil in stretch-resistant vaso-occlusive coils

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Quick Facts
Patent No.
US 7,485,122
App. No.
10/185,671
Granted
Feb 3, 2009
Kind
B2
Abstract

Vaso-occlusive devices are provided for occluding an aneurysm within the human vasculature. The vaso-occlusive device also includes a stretch-resisting member that extends through at least a portion of a lumen of the primary coil and is directly or indirectly attached to the primary coil at two locations axially separated from each other to prevent or minimize axial stretching of the primary coil. At one location, the stretch-resisting member is coupled to the primary coil via a flexible anchor assembly disposed within the lumen. The anchor coil is incorporated into the primary coil by disposing the anchor coil windings between the windings of the primary coil.

Claims (37)

1. A vaso-occlusive device, comprising:

a primary coil having a proximal end, a distal end, and a lumen, the primary coil comprising windings;

a stretch-resisting member extending through at least a portion of the coil lumen and being coupled to the primary coil; and

an anchor assembly fixedly coupled with the primary coil, the anchor assembly comprising an anchor coil having windings inter-wound between the primary coil windings, wherein the primary coil and anchor coil have approximately the same diameter.

2. The device of claim 1 , wherein the anchor coil is directly attached to the stretch-resisting member.

3. The device of claim 1 , wherein each winding of the anchor coil is disposed between adjacent windings of the primary coil.

4. The device of claim 1 , wherein at least two windings of the anchor coil are disposed between adjacent windings of the primary coil.

5. The device of claim 1 , wherein the stretch-resisting member comprises at least one polymeric filament.

6. The device of claim 1 , wherein a distal end of the stretch-resisting member is coupled to the distal end of the primary coil and a proximal end of the stretch-resisting member is coupled to the anchor coil.

7. The device of claim 6 , wherein the distal end of the stretch-resisting member is directly attached to the distal end of the primary coil.

8. The device of claim 1 , wherein the anchor assembly is coupled to the proximal end of the primary coil.

9. The device of claim 1 , further comprising a deployment mechanism coupled to the proximal end of the anchor coil.

10. The device of claim 9 , wherein the deployment mechanism comprises an electrolytically severable junction adapted to detach from a core wire by imposition of an electrical current on the core wire.

11. The device of claim 1 , wherein all of the windings of the anchor coil are disposed between the windings of the primary coil.

12. The device of claim 1 , wherein the primary coil is sized to fit within an aneurysm.

13. The device of claim 1 , wherein the primary coil windings are spaced, such that a substantial axial stress is not exerted on the primary coil windings and anchor coil windings.

14. The device of claim 1 , wherein the anchor coil has a proximal winding, a distal winding, and one or more intermediate windings between the proximal and distal windings, and wherein no portion of the one or more intermediate anchor coil windings is disposed in the coil lumen.

15. The device of claim 1 , wherein the anchor coil is approximately 2 mm long.

16. A catheter assembly for occluding a body cavity comprising:

a delivery device having a distal end; and

a vaso-occlusive device associated with the distal end of the delivery device, the vaso-occlusive device comprising:

a primary coil having a proximal end, a distal end, and a lumen, the primary coil comprising windings;

a stretch-resisting member extending through at least a portion of the coil lumen and being coupled to the primary coil; and

an anchor assembly fixedly coupled with the primary coil, the anchor assembly comprising an anchor coil having windings inter-wound between the primary coil windings, wherein the primary coil and anchor coil have approximately the same diameter.

17. The catheter assembly of claim 16 , wherein the anchor coil is directly attached to the stretch-resisting member.

18. The catheter assembly of claim 16 , wherein each winding of the anchor coil is disposed between adjacent windings of the primary coil.

19. The catheter assembly of claim 16 , wherein at least two windings of the anchor coil are disposed between adjacent windings of the primary coil.

20. The catheter assembly of claim 16 , wherein the stretch-resisting member comprises at least one polymeric filament.

21. The catheter assembly of claim 16 , wherein a distal end of the stretch-resisting member is coupled to the distal end of the primary coil and a proximal end of the stretch-resisting member is coupled to the anchor coil.

22. The catheter assembly of claim 21 , wherein the distal end of the stretch-resisting member is directly attached to the distal end of the primary coil.

23. The catheter assembly of claim 16 , wherein the anchor assembly is coupled to the proximal end of the primary coil.

24. The catheter assembly of claim 16 , wherein the vaso-occlusive coil is detachably connected via an electrolytic joint.

25. The catheter assembly of claim 16 , wherein the body cavity comprises an aneurysm.

26. The catheter assembly of claim 16 , further comprising a catheter, wherein the delivery device is a core wire slidably disposed within the catheter, wherein the vaso-occlusive device is detachably coupled to the core wire.

27. The catheter assembly of claim 16 , wherein the primary coil windings are spaced, such that a substantial axial stress is not exerted on the primary coil windings and anchor coil windings.

28. The catheter assembly of claim 16 , wherein the anchor coil has a proximal winding, a distal winding, and one or more intermediate windings between the proximal and distal windings, and wherein no portion of the one or more intermediate anchor coil windings is disposed in the coil lumen.

29. The catheter assembly of claim 16 , wherein the anchor coil is approximately 2 mm long.

Assignments (7)
CHANGE OF ADDRESS Recorded Dec 18, 2024
From: STRYKER CORPORATION
To: STRYKER CORPORATION
Reel/Frame 069737/0184 →
CHANGE OF ADDRESS Recorded Dec 18, 2024
From: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
To: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
Reel/Frame 069730/0754 →
NUNC PRO TUNC ASSIGNMENT Recorded Jun 7, 2020
From: STRYKER EUROPEAN HOLDINGS I, LLC
To: STRYKER EUROPEAN HOLDINGS III, LLC
Reel/Frame 052861/0001 →
CHANGE OF NAME Recorded Jun 7, 2020
From: STRYKER EUROPEAN HOLDINGS III, LLC
To: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
Reel/Frame 052860/0716 →
NUNC PRO TUNC ASSIGNMENT Recorded Nov 23, 2015
From: STRYKER NV OPERATIONS LIMITED
To: STRYKER MEDTECH LIMITED
Reel/Frame 037153/0034 →
NUNC PRO TUNC ASSIGNMENT Recorded Nov 23, 2015
From: STRYKER MEDTECH LIMITED
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 037153/0241 →
CHANGE OF NAME Recorded Nov 6, 2006
From: SCIMED LIFE SYSTEMS, INC.
To: BOSTON SCIENTIFIC SCIMED, INC.
Reel/Frame 018505/0868 →