IP Library Granted Patent US 8,992,563
Granted Patent B2
US 8,992,563 · App. 12/913,177 · Granted Mar 31, 2015

Delivery wire assembly for occlusive device delivery system

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Quick Facts
Patent No.
US 8,992,563
App. No.
12/913,177
Granted
Mar 31, 2015
Kind
B2
Abstract

A delivery wire assembly for delivering an occlusive device to a location in a patient's vasculature, includes delivery wire conduit defining a conduit lumen, a core wire disposed in the conduit lumen, the core wire having a distal detachment zone, and an enhancing coil disposed around the distal detachment zone, the enhancing coil configured to transfer a distally directed force from the delivery wire assembly to objects located distal of the delivery wire assembly without damaging the distal detachment zone. In one embodiment, the enhancing coil includes a proximal section having a first diameter, a distal section having a diameter larger than the diameter of the proximal section, and a transition section connecting the respective proximal and distal sections, wherein the transition section flares radially in a distal direction.

Claims (36)

1. A delivery wire assembly for delivering an occlusive device to a location in a patient's vasculature, comprising:

a delivery wire conduit defining a conduit lumen;

a core wire disposed in the conduit lumen, the core wire having a distal detachment zone; and

an enhancing coil disposed around the distal detachment zone, the enhancing coil comprising

a proximal section having a first diameter, the proximal section being secured by an adhesive to an inner surface of the conduit lumen and to the core wire, thereby forming a watertight seal,

a distal section having a diameter larger than the diameter of the proximal section, and

a transition section connecting the respective proximal and distal sections, wherein the transition section flares radially in a distal direction,

wherein the enhancing coil is configured to transfer a distally directed force from the delivery wire assembly to objects located distal of the delivery wire assembly without damaging the distal detachment zone.

2. The delivery wire assembly of claim 1 , wherein at least a portion of the proximal section of the enhancing coil is disposed in the conduit lumen.

3. The delivery wire assembly of claim 1 , wherein the enhancing coil is electrically connected to the delivery wire conduit.

4. The delivery wire assembly of claim 3 , wherein the enhancing coil forms a portion of a cathode of an electrolytic detachment circuit.

5. The delivery wire assembly of claim 1 , wherein the distal section of the enhancing coil has an open pitch.

6. A system for delivering an occlusive device to a location in a patient's vasculature, comprising:

a delivery catheter defining a catheter lumen;

a delivery wire assembly configured to be slidably inserted into and through the lumen of the delivery catheter, the delivery wire assembly comprising

a delivery wire conduit defining a conduit lumen,

a core wire disposed in the conduit lumen, the core wire having a distal detachment zone, and

an enhancing coil disposed around the distal detachment zone, the enhancing coil comprising

a proximal section having a diameter, the proximal section being secured by an adhesive to an inner surface of the conduit lumen and to the core wire, thereby forming a watertight seal,

a distal section having a diameter larger than the diameter of the proximal section, and

a transition section connecting the respective proximal and distal sections, wherein the transition section flares radially in a distal direction;

an occlusive device detachably connected to the distal detachment zone; and

a power supply electrically connected to the delivery wire assembly, wherein the enhancing coil is not directly attached to the occlusive device,

wherein the enhancing coil is configured to transfer a distally directed force from the delivery wire assembly to push the occlusive device through a patient's vasculature without damaging the distal detachment zone.

7. The occlusive device delivery system of claim 6 , wherein at a least portion of the proximal section of the enhancing coil is disposed in the conduit lumen.

8. The occlusive device delivery system of claim 6 , wherein the enhancing coil is electrically connected to the delivery wire conduit, and the enhancing coil forms a portion of a cathode of an electrolytic detachment circuit.

9. The occlusive device delivery system of claim 6 , wherein the distal section of the enhancing coil has an open pitch.

10. A delivery wire assembly for delivering an occlusive device to a location in a patient's vasculature, comprising:

a delivery wire conduit defining a conduit lumen;

a core wire disposed in the conduit lumen, the core wire having a distal detachment zone; and

an enhancing coil disposed around the distal detachment zone, the enhancing coil comprising

a proximal section having a first diameter, the proximal section being secured by an adhesive to an inner surface of the conduit lumen and to the core wire, thereby forming a watertight seal,

a distal section having a diameter larger than the diameter of the proximal section, and

a transition section connecting the respective proximal and distal sections, wherein the enhancing coil is electrically connected to the delivery wire conduit and forms a portion of a cathode of an electrolytic detachment circuit, wherein the distal section of the enhancing coil has an open pitch, and wherein the enhancing coil is configured to transfer a distally directed force from the delivery wire assembly to objects located distal of the delivery wire assembly without damaging the distal detachment zone.

11. The delivery wire assembly of claim 10 , wherein the transition section flares radially in a distal direction.

12. The delivery wire assembly of claim 10 , wherein at least a portion of the proximal section of the enhancing coil is disposed in the conduit lumen.

Assignments (7)
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 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 →
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 →
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 24, 2011
From: BOSTON SCIENTIFIC SCIMED, INC.
To: STRYKER CORPORATION; STRYKER NV OPERATIONS LIMITED
Reel/Frame 026018/0579 →