The University of Texas System

Other

Micro Therapeutics, Inc.

Idev Technologies, Inc.

William Cook, Europe A/s

William Cook Europe S.a.

Kenneth Carroll Wright

Sidney Wallace

Andras Konya

Hideki Hyodoh

Dusan Pavcnik

Andr&aacute;s K&oacute;nya

Andres Konya

András Kónya

Self-expandable, woven intravascular devices for use as stents (both straight and tapered), filters (both temporary and permanent) and occluders for insertion and implantation into a variety of anatomical structures. The devices may be formed from shape memory metals such as nitinol. The devices may also be formed from biodegradable materials. Delivery systems for the devices include two hollow tubes that operate coaxially. A device is secured to the tubes prior to the implantation and delivery of the device by securing one end of the device to the outside of the inner tube and by securing the other end of the device to the outside of the outer tube. The stents may be partially or completely covered by graft materials, but may also be bare. The devices may be formed from a single wire. The devices may be formed by either hand or machine weaving. The devices may be created by bending shape memory wires around tabs projecting from a template, and weaving the ends of the wires to create the body of the device such that the wires cross each other to form a plurality of angles, at least one of the angles being obtuse. The value of the obtuse angle may be increased by axially compressing the body.

Plain woven stents

Methods for treating femoro-popliteal artery of a patient include delivering a self-expanding, woven stent from a delivery system. The methods may include delivering a guidewire to a lesion in the femoro-popliteal artery stem over the guidewire.

Self expandable, woven intravascular devices for use as stents (both straight and tapered), filters (both temporary and permanent) and occluders for insertion and implantation into a variety of anatomical structures. The devices may be formed from shape memory metals such as nitinol. The devices may also be formed from biodegradable materials. Delivery systems for the devices include two hollow tubes that operate coaxially. A device is secured to the tubes prior to the implantation and delivery of the device by securing one end of the device to the outside of the inner tube and by securing the other end of the device to the outside of the outer tube. The stents may be partially or completely covered by graft materials, but may also be bare. The devices may be formed from a single wire. The devices may be formed by either hand or machine weaving. The devices may be created by bending shape memory wires around tabs projecting from a template, and weaving the ends of the wires to create the body of the device such that the wires cross each other to form a plurality of angles, at least one of the angles being obtuse. The value of the obtuse angle may be increased by axially compressing the body.

Methods for creating woven devices

Woven intravascular devices and methods for making the same and apparatus for delivery of the same

An occlusion method and apparatus. The occluder includes elastically deformable members and a jacket. The elastically deformable members are secured in spaced relation and extend in arcuate conformation therebetween. The jacket covers at least a portion of the elastically deformable members. The elastically deformable members are configured to become compressed upon application of a force and to recover the arcuate conformation upon removal of the fore to occlude a site.

Occlusion method and apparatus

A coil-type vasoocclusion device ( ) for establishing an embolus or vascular occlusion in a human or veterinary patient is adapted for introduction into the patient via a catheter ( ). The device ( ) first includes a coil ( ) having proximal and distal coil ends ( ) and a coil lumen ( ). The device ( ) also includes a core ( ) disposed in at least part of the coil lumen ( ), the core having proximal and distal core ends ( ). Only one core end ( or ) is directly affixed to a respective end ( or ) of the coil ( ); the other core end ( or ) is not directly connected to either end ( or ) of the coil ( ). The core ( ) is preferably nitinol in a superelastic state, being in other than its stress induced, martensitic condition. The device ( ) can include a thrombogenic material ( ) connected to or carried by the coil ( ). The coil ( ) is preferably adapted to achieve a suitable secondary shape ( ) when deployed from the catheter ( ). A medical device ( ) combining the catheter ( ), a pusher ( ), a coupling ( ) and the vasoocclusion device ( ) is also disclosed. The vasoocclusion device ( ) is easily repositioned in the vascular system, thereby ensuring proper deployment, and also enjoys a dislodging force about twice as great as comparable coil-type devices lacking the core ( ), substantially or completely preventing migration of the device ( ) after its deployment.

Vasoocclusion coil device having a core therein

A wire frame stent and stent delivery system for inserting the stent into the body.

Hoop stent

A retrieval device or snare for grasping foreign articles and retrieving them from the body of a patient. The retrieval device includes a catheter open at both ends such that it may be advanced along a guidewire. The distal end of a wire is attached to the first catheter near an opening system within the catheter. The opening system may be a slot or a pair of holes. A portion of the wire is oriented external of the catheter. Manipulation of the proximal end of the wire causes a portion of the wire to form a loop external of the catheter. The catheter may be tapered, as may be the wire. A reinforcing- material may be attached to the portion of the wire that forms the loop. Another reinforcing material may also be attached to the proximal portion of the wire in order to stiffen the wire and improve its pushability. A guidewire may be inserted into a patient and maneuvered to an appropriate location within the patient, the catheter may be advanced over the guidewire, the wire attached to the catheter may be manipulated to capture a foreign body with the loop, and the catheter and foreign body may be withdrawn from the patient.

Foreign body retrieval device

Bifurcated and trifurcated woven stents for insertion and delivery into a variety of anatomical structures, including the aortic-iliac bifurcation, the superior vena cava junction, and the inferior vena cava junction. The bifurcated stents includes a first leg formed from a first plurality of wires, a second leg formed from a second plurality of wires, and a common body formed from the first and second pluralities of wires. The wires may be nitinol. Biodegradable filaments may also be utilized. The angles created between the crossed wires is preferably obtuse. A variety of delivery devices formed from differently-sized tubes, portions of which may operate co-axially with each other, are also included. The bifurcated stents may be formed from as few as two wires. The stents may be formed using plain weaving effected either by hand or by machine.

Woven bifurcated and trifurcated stents and methods for making the same

An occlusion method and apparatus. The occluder includes a elastically deformable members and a jacket. The elastically deformable members are secured in spaced relation and extend in arcuate conformation therebetween. The jacket covers at least a portion of the elastically deformable members. The elastically deformable members are configured to become compressed upon application of a force and to recover the arcuate conformation upon removal of the force to occlude a site.

A declotting method and apparatus. A declotting apparatus includes a catheter, a member positioned within the catheter, and a plurality of deformable members. The plurality of members bow and compress as the catheter slides relative to the member so that a site may be declotted. In another embodiment, a declotting apparatus includes a first and second catheter, a guidewire, a deformable jacket, and a liner. The deformable jacket expands and contracts as the first catheter slides relative to the second catheter so that a site may be declotted. The guidewire facilitates navigation, and the liner prevents material from entering the apparatus.

Growing community of inventors

Houston, TX, United States of America

Kenneth Carroll Wright