IP Library Granted Patent US 9,636,115
Granted Patent B2
US 9,636,115 · App. 11/423,934 · Granted May 2, 2017

Vaso-occlusive delivery device with kink resistant, flexible distal end

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Quick Facts
Patent No.
US 9,636,115
App. No.
11/423,934
Granted
May 2, 2017
Kind
B2
Abstract

A device for delivering an occlusive element includes an elongate sheath having a lumen therein. An elongate core member is disposed within the lumen and is formed from a proximal portion and distal portion connected via a joint. The distal portion of the elongate member includes a severable junction secured to the occlusive element. A marker coil is coaxially arranged around the distal portion of the elongate core member and is partially disposed inside the sheath lumen. A coil member is coaxially arranged around the distal portion of the elongate core member and coaxially arranged around at least a portion of the marker coil extending outside the lumen of the sheath. The coil member is secured at a distal end thereof to the distal portion of the elongate core member. The device resists axial compression while allowing for radial bending.

Claims (30)

1. A vaso-occlusive assembly, comprising:

an elongate sheath having a wall and defining an axial lumen;

respective proximal and distal elongate core members disposed within the lumen of the sheath, wherein the proximal elongate core member is joined to the distal elongate core member at a joint located within the sheath lumen, the distal elongate core member including a severable junction;

a marker coil coaxially arranged around the distal elongate core member and partially disposed within the lumen of the sheath;

a coil member coaxially arranged around the distal elongate core member and further coaxially arranged around at least a portion of the marker coil, the coil member further being secured at a distal end thereof to the distal elongate core member; and

a vaso-occlusive coil coupled to the distal elongate core member at a location distal to the severable junction.

2. The assembly of claim 1 , wherein the distal elongate core member includes a hook that is secured to one or more proximal windings of the vaso-occlusive coil.

3. The assembly of claim 2 , wherein the interface between the hook and the one or more proximal windings of the vaso-occlusive coil is covered with an adhesive.

4. The assembly of claim 2 , wherein the one or more proximal windings are crimped about a portion of the hook.

5. The assembly of claim 2 , further comprising a stretch resistant filament secured at one end to the hook and at another end to the vaso-occlusive coil.

6. The assembly of claim 1 , further comprising a delivery catheter defining an axial lumen, the vaso-occlusive assembly being slidable through the lumen of the delivery catheter.

7. The assembly of 1 , wherein the coil member is secured to the distal elongate core member via a stopper coil and adhesive.

8. The assembly of claim 1 , wherein the joint is contained within a segment of hypotube.

9. A vaso-occlusive assembly, comprising:

an elongate sheath having a wall and defining an axial lumen therethrough;

an elongate core member disposed within the lumen of the sheath, the elongate core member including a proximal portion joined to a distal portion at a joint, the distal portion including a severable junction;

a spacer member coaxially arranged around the distal portion of the elongate core member and disposed within the lumen of the sheath at a location distal to the joint;

a marker coil coaxially arranged around the distal portion of the elongate core member and disposed within the lumen of the sheath at a location distal to the spacer member;

a coil member coaxially arranged around the distal portion of the elongate core member and at least a portion of the marker coil, the coil member further being secured at a distal end thereof to the distal portion of the elongate core member; and

a vaso-occlusive coil coupled to the distal portion of the core member at a location distal to the severable junction.

10. The assembly of claim 9 , wherein the coil member is secured to the distal portion of the elongate core member via a stopper coil and adhesive.

11. The assembly of claim 9 , wherein the joint is contained within a segment of hypotube.

12. The assembly of claim 9 , wherein the spacer member comprises a polyimide material.

13. The assembly of claim 9 , wherein the distal portion of the core member in the region of the severable junction has a diameter within the range of about 0.001″ to about 0.0025″.

14. The assembly of claim 9 , wherein the coil member comprises a stainless steel coil.

15. The assembly of claim 9 , wherein the distal portion of the core member includes a hook that is secured to one or more proximal windings of the vaso-occlusive coil.

16. The assembly of claim 15 , wherein the interface between the hook and the one or more proximal windings of the vaso-occlusive coil is covered with an adhesive.

17. The assembly of claim 15 , wherein the one or more proximal windings are crimped about a portion of the hook.

18. The assembly of claim 15 , further comprising a stretch resistant filament secured at one end to the hook and at another end to the vaso-occlusive coil.

19. The assembly of claim 15 , further comprising a delivery catheter defining an axial lumen therethrough, the vaso-occlusive assembly being slidable through the lumen of the delivery catheter.

Assignments (9)
CHANGE OF ADDRESS Recorded Dec 18, 2024
From: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
To: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
Reel/Frame 069730/0754 →
CHANGE OF ADDRESS Recorded Dec 18, 2024
From: STRYKER CORPORATION
To: STRYKER CORPORATION
Reel/Frame 069737/0184 →
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 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT SERIAL # 09/905,670 AND 07/092,079 PREVIOUSLY RECORDED AT REEL: 037153 FRAME: 0034. ASSIGNOR(S) HEREBY CONFIRMS THE NUNC PRO TUNC ASSIGNMENT. Recorded Mar 8, 2016
From: STRYKER NV OPERATIONS LIMITED
To: STRYKER MEDTECH LIMITED
Reel/Frame 038039/0001 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT LISTED SERIAL NOS. 09/905,670 AND 07/092,079 PREVIOUSLY RECORDED AT REEL: 037153 FRAME: 0241. ASSIGNOR(S) HEREBY CONFIRMS THE NUNC PRO TUNC ASSIGNMENT EFFECTIVE DATE 9/29/2014. Recorded Mar 8, 2016
From: STRYKER MEDTECH LIMITED
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 038043/0011 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2011
From: BOSTON SCIENTIFIC SCIMED, INC.
To: STRYKER CORPORATION; STRYKER NV OPERATIONS LIMITED
Reel/Frame 025969/0841 →