IP Library Granted Patent US 9,060,777
Granted Patent B1
US 9,060,777 · App. 14/289,555 · Granted Jun 23, 2015

Vaso-occlusive devices and methods of use

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Quick Facts
Patent No.
US 9,060,777
App. No.
14/289,555
Granted
Jun 23, 2015
Kind
B1
Abstract

Vaso-occlusive apparatuses, including implants, and methods of using them to treat aneurysms. For example, described herein are expandable vaso-occlusive implants that include one or more soft and expandable braided member coupled to a pushable member such as a coil that maybe inserted and retrieved from within an aneurism using a delivery catheter. In particular, the expandable implants described herein are configured to allow relatively soft and elongate implants to be pushed out of a cannula without binding up within the cannula.

Claims (34)

1. A vaso-occlusion system for occluding an aneurysm, the system comprising:

a delivery catheter extending from a proximal end to a distal end; and

a vaso-occlusive device within the delivery catheter, wherein the vaso-occlusive device is adapted to be pushed out of, and retrieved back into, the distal end of the delivery catheter, the vaso-occlusive device comprising:

an elongate inner member having a diameter;

a soft outer braided tubular member formed of about 24 to 36 strands comprising a Nitinol wire having a thickness that is 0.0010 inches or less in diameter, wherein the braided tubular member is attached and fixed to the inner member at a proximal end of the braided tubular member and extends in a longitudinal axis over the inner member but is not attached to the inner member at a distal end of the braided tubular member, further wherein the braided tubular member has a length that is greater than 5 cm, forms a braid angle between crossing strands in a direction of the longitudinal axis of about 35 degrees or less when held within the delivery catheter, and expands relative to the inner member to a diameter of greater than 1.5 times the diameter of the inner member when released from the delivery catheter.

2. The vaso-occlusion system of claim 1 , further comprising a pusher connected to the vaso-occlusive device.

3. The vaso-occlusion system of claim 1 , wherein the strands comprise a monofilament wire having a thickness that is less than about 0.0008 inches diameter.

4. The vaso-occlusion system of claim 1 , wherein the strands comprise a Nitinol wire having a thickness that is between about 0.0004 and 0.00075 inches diameter.

5. The vaso-occlusion system of claim 1 , wherein the inner member comprises a closed pitch coil.

6. The vaso-occlusion system of claim 1 , wherein the inner member comprises a platinum coil.

7. The vaso-occlusion system of claim 1 , wherein the braided tubular member comprises a braid angle of 30 degrees or less when held within the delivery catheter.

8. The vaso-occlusion system of claim 1 , further comprising a second outer braided tubular member that is attached to the inner member proximal to the outer braided/braided tubular member.

9. The vaso-occlusion system of claim 1 , wherein the braided tubular member is configured to have an expanded braid angle between about 35-90 degrees and a diameter between about 0.75 mm to about 3.0 mm.

10. The vaso-occlusion system of claim 1 , wherein the braided tubular member is configured to have an expanded braid angle less than about 50 degrees and a diameter between about 0.75 mm to about 3.0 mm.

11. The vaso-occlusion system of claim 1 , wherein the braided tubular member has a pore size formed between strands in the expanded configuration of less than about 0.1 square mm.

12. The vaso-occlusion system of claim 1 , wherein the braided tubular member is configured to have a pre-set transverse shape that is non-circular.

13. The vaso-occlusion system of claim 1 , wherein the braided tubular member is configured to have a pre-set to a 3D configuration.

14. The vaso-occlusion system of claim 1 , wherein an elongate length of the vaso-occlusive device is configured to have a pre-set curve or shape.

15. The vaso-occlusion system of claim 1 , wherein the proximal end of the braided tubular member is bound to the inner member by a polymeric junction or a metallic weld.

16. The vaso-occlusion system of claim 1 , wherein the braided tubular member has a length that is less than about 45 cm.

17. The vaso-occlusion system of claim 1 , wherein the catheter has an inner diameter of between about 0.015 inches and about 0.025 inches.

18. The vaso-occlusion system of claim 1 , wherein the catheter has an inner diameter of between about 0.015 inches and about 0.018 inches.

19. A vaso-occlusion device for occluding an aneurysm, wherein the vaso-occlusion device comprises a collapsed configuration that is pushable out of a delivery catheter and an expanded configuration, the vaso-occlusive device further comprising:

an elongate inner member having a diameter; and

a soft outer braided tubular member formed of about 24 to 36 strands comprising a Nitinol wire having a thickness that is 0.0010 inches or less in diameter, wherein the braided tubular member is attached and fixed to the inner member at a proximal end of the braided tubular member and extends in a longitudinal axis over the inner member but is not attached to the inner member at a distal end of the braided tubular member, further wherein the braided tubular member has a length that is greater than 5 cm, forms a braid angle between crossing strands in a direction of the longitudinal axis of about 35 degrees or less in the collapsed configuration within the delivery catheter, and expands relative to the inner member to a diameter of greater than 1.5 times the diameter of the inner member in the expanded configuration when released from the delivery catheter.

20. A method of occluding an aneurysm in a patient, the method comprising:

inserting a catheter into the patient, wherein the catheter houses a vaso-occlusive device in a collapsed configuration within a lumen of the catheter, and the vaso-occlusive device comprises an elongate inner member having a diameter and an outer braided tubular member formed of about 24 to 36 strands comprising a Nitinol wire having a thickness that is 0.0010 inches or less in diameter, wherein the braided tubular member is attached and fixed to the inner member at a proximal end of the braided tubular member and extends in a longitudinal axis over the inner member but is not attached at a distal end of the braided tubular member, further wherein the braided tubular member has a length that is greater than 5 cm, and the braided tubular member forms a braid angle between crossing strands in a direction of the longitudinal axis of about 35 degrees or less in the collapsed configuration within the catheter; and

pushing the vaso-occlusive device distally out of the catheter so that the braided tubular member expands relative to the inner member to a diameter of greater than 1.5 times the diameter of the inner member in an expanded configuration when released from the delivery cannula.

21. The method of claim 20 , further comprising detaching a distal length of the vaso-occlusive device from the proximal end of the vaso-occlusive device.

22. The method of claim 20 , further comprising retrieving at least a portion of the vaso-occlusive device that has been pushed out of the catheter back into the catheter by retracting the vaso-occlusive device proximally into the catheter.

23. The method of claim 20 , further comprising retrieving at least a portion of the vaso-occlusive device that has been pushed out of the catheter back into the catheter by retracting the vaso-occlusive device proximally into the catheter, and then again pushing the vaso-occlusive device distally out of the catheter.

24. The method of claim 20 , wherein the vaso-occlusive device is pre-biased in a curve so that it bends as it is pushed out of the catheter to assume three-dimensional shape.

25. The method of claim 20 , further comprising positioning a distal end region of the catheter adjacent an aneurysm in the body before pushing the vaso-occlusive device out of the catheter.

26. The method of claim 20 , further comprising limiting the flow of blood through the vaso-occlusive device when inserted into the patient after being pushed from the catheter by a small pore size formed between strands in the expanded configuration that are less than about 0.1 square mm.

Assignments (6)
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 Jul 23, 2021
From: STRYKER EUROPEAN HOLDINGS I, LLC
To: STRYKER EUROPEAN HOLDINGS III, LLC
Reel/Frame 056969/0771 →
CHANGE OF NAME Recorded Jul 23, 2021
From: STRYKER EUROPEAN HOLDINGS III, LLC
To: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
Reel/Frame 056969/0893 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME PREVIOUSLY RECORDED ON REEL 036217 FRAME 0473. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 1, 2017
From: TW MEDICAL TECHNOLOGIES, LLC
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 041582/0574 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 30, 2015
From: TW MEDICAL TECHNOLOGIES, LLC
To: STRYKER EUROPEAN HOLDINGS I, LLC, IN ITS CAPACITY AS SOLE GENERAL PARTNER OF STRYKER EUROPEAN TECHNOLOGIES C.V.
Reel/Frame 036217/0473 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2015
From: WALLACE, MICHAEL P.; GREENHALGH, E. SKOTT
To: TW MEDICAL TECHNOLOGIES, LLC
Reel/Frame 035473/0886 →