Cordis Corporation

Depuy Synthes Products, Inc.

Cardinal Health Switzerland 515 Gmbh

Donald Francis Depalma

Clifford J. Dwyer

Kirk L. Johnson

Alfredo Castaneda

Robert Burgermeister

Mark N. Inderbitzen

Isaac John Khan

David C. Majercak

Scott Lyle Rush

Michael Dugery

Donald D. Boucher

Kirk L Johnson

Juan A Lorenzo

Mark N Inderbitzen

David Christopher Majercak

Roberto Echarri

Lacey Gorochow

Robert R Slazas

Stephen J Querns

David J Wilson

Pedro L Diaz

Dillon Karg

Patrick O'Neill

Donald D Boucher

Craig L Bonsignore

Luis A Davila

Noah M Roth

Clifford Dwyer

Robert Lulo

Frederick Feller, Iii

Susana M Martinez

Donald Francis DePalma

Melissa Clinger

Melissa Querns, Legal Representative

Thomas Wiatrowski

Merril L Knudtson

Pedro Diaz

Bruce A Hoo

David Wilson

Clifford J Dwyer

A clot retrieval cleaning instrument can have bristles, fluid sprays, or other techniques to liberate captured clot material from a clot retrieval device so that it can be reinserted into a patient's vasculature for successive capture attempts. The cleaning instrument can be conveniently integrated or connected to a hemo stasis valve assembly so that the cleaning function can be performed without completely removing the clot retrieval device from the delivery system. Aspiration can be applied to remove the freed thrombus material. The cleaning instrument can be removable from the delivery system to facilitate the instrument's washing or disposal.

Clot retriever cleaning for reinsertion

The disclosed technology includes a detachment system for delivering an implantable medical device to a target location of a body vessel including a proximal delivery tube, a distal delivery tube, and a braid segment disposed between. The distal tube includes a proximal end, a distal end, and a compressible portion of the tube itself, between the proximal and distal ends which is axially movable from a compressed to an elongated condition. The proximal tube has a proximal end and a distal end. The braid segment is formed from a plurality of wires. An engagement system engages and deploys the implantable medical device engaged at the distal end of the distal tube.

Implantable medical device detachment system with flexible braid section

The helical balloon assist device includes a tubular balloon formed at least partially into an independent helical shape in an uninflated state and an inflation tube in sealed communication with the balloon and extending from the helical balloon assist device in a proximal direction. The helical balloon assist device may include an inner core member formed at least partially into an independent helical shape and supporting the helical shape of the tubular balloon.

Helical balloon assist device and method for using the same

A device for capturing an obstruction in a vasculature can include an expandable braid, an invertible braid, and elongated members such as tubes or wires that can be moved to cause the expandable braid to expand and the invertible braid to form a pocket facing toward the expandable braid to thereby capture the obstruction within the pocket. The expandable braid can form a cap at an open end of the pocket so that the pocket and cap define a cavity in which the obstruction can be confined. The device can also have an expandable framework between the expandable braid and the invertible braid that can engage the obstruction to further secure the obstruction between the expandable braid and invertible braid.

Vasculature obstruction capture device

A method of delivering a catheter to a location of interest in the vasculature, the method including positioning a self-expanding sheath within a lumen of the catheter; advancing the catheter and the self-expanding sheath in tandem over a guidewire; and distally moving a distal end of the self-expanding sheath out from the lumen of the catheter thereby causing the self-expanding sheath to move from a collapsed state within the catheter to an expanded state outside the catheter, wherein when the self-expanding sheath is in the expanded state both the self-expanding sheath and the catheter are distally advanceable in tandem.

System and method for delivering a catheter

A clot retrieval cleaning instrument can have bristles, fluid sprays, or other techniques to liberate captured clot material from a clot retrieval device so that it can be reinserted into a patient's vasculature for successive capture attempts. The cleaning instrument can be conveniently integrated or connected to a hemostasis valve assembly so that the cleaning function can be performed without completely removing the clot retrieval device from the delivery system. Aspiration can be applied to remove the freed thrombus material. The cleaning instrument can be removable from the delivery system to facilitate the instrument's washing or disposal.

A single integrated intravascular device including a stentriever and semi-compliant balloon housed therein. After traversing a clot, the device is deployed to a self-expanded state engaging the clot therein, whereupon the device along with the embedded clot is removed. Detecting through imaging a stenosis at an original position of the captured clot, the device is reintroduced to that location and the stentriever is deployed to a self-expanded state. Inflating the semi-compliant balloon enlarges the stentriever to a hyper-expanded state greater than the self-expanded state thereby dilating the vessel while simultaneously completely detaching/releasing the stentriever from a remaining portion of the device. Then the semi-compliant balloon is collapsed and withdrawn along with the remaining portion of the device, while the detachable/releasable portion of the stentriever in the self-expanded state remains in the vessel.

Streamlined treatment of clot removal, angioplasty and prevention of restenosis using a single integrated intravascular device

Implant deployment systems can generally can include a braided implant that can be detachably attached to a delivery tube by an expansion ring that can be positioned within a notch on an outer surface of the delivery tube near a distal end of the delivery tube. The implant can be positioned within a lumen of the delivery tube and remain attached to the delivery tube as the assembly is fed through a microcatheter to a treatment site. Once the braided implant is implanted, the expansion ring can move from a collapsed configuration that is engaged with the notch of the delivery tube to a deployed configuration that releases the delivery tube, thereby releasing the braided implant from the delivery tube.

Intrasaccular device positioning and deployment system

Systems and methods for delivering a catheter to a location of interest in the vasculature, the method including selectively positioning a guidewire at the location, positioning a self-expanding sheath within a lumen of the catheter, advancing the catheter and the self-expanding sheath in tandem over the guidewire, and distally moving a distal end of the self-expanding sheath out from an inner lumen of the catheter thereby causing the self-expanding sheath to move from a collapsed state within the catheter to an expanded state outside the catheter.

A device for capturing an obstruction in a vasculature can include a first elongated member, an expandable element, an invertible element, and a gap positioned between the expandable element and the invertible element sized to be placed across the obstruction. The expandable element and the invertible element can be positioned near the distal end of the first elongated member. The expandable element can expand from a collapsed delivery configuration to an expanded configuration. The invertible element can expand from a collapsed delivery configuration to an expanded configuration, and the invertible element can invert from the expanded configuration to an inverted configuration, thereby forming a pocket. The pocket can envelope at least a portion of the gap and can thereby capture an obstruction that is in the gap.

An embolic coil detachment system includes an elongated, flexible shape memory polymer tube having an inner wall surface defining an interior lumen. A distal portion of the shape memory polymer tube has an enlarged and reduced diameter configurations. An embolic coil is releasably mounted to the shape memory polymer tube by a headpiece releasably attached within a distal portion of the shape memory polymer tube. A resistive heating element disposed longitudinally along and in immediate contact with the inner wall surface of the distal tubular wall of the shape memory polymer tube provides direct, even heating to release the headpiece and embolic coil attached thereto when the resistive heating element is energized.

Embolic coil detachment mechanism with flexible distal member, resistive electrical heating element and shape memory polymer element

A detachment actuator for use with an implantable medical device deployment system that guide and deploys the medical device at a target location within a body vessel. The detachment actuator includes a first portion that is connected the implantable medical device and a second portion that is attached to a control member the controls the release of the medical device, The second portion of the detachment actuator detaches and moves away from the first portion of the detachment actuator to move the control member and release the medical device.

Detachment actuator for use with medical device deployment systems

An endoprosthetic device for treating abdominal aortic aneurysms using suprarenal fixation. A stent ring is anchored in an area above the renal arties using self-flaring barbs that project during the nitinol expansion process. Sutures extend from the stent ring to an area below the renal arties to a bifurcated trunk portion comprising a nitinol fabric on a non-kinking frame. The bifurcated trunk is sealed proximal the iliac arteries and includes iliac leg holders having self-flaring retention struts for non-traumatic holding of iliac leg prosthetics. Suprarenal fixation and collapsible cells having retention projections and barbs that only flare during the nitinol expansion process assist in lowering the devices profile and sheathability for percutaneous delivery and may provide for recapturing the anchored device.

Percutaneous endoprosthesis using suprarenal fixation and barbed anchors

The present invention is directed to a prosthesis and method for treating, repairing, and/or replacing an abdominal aortic aneurysm. The prosthesis includes a coiled stent comprised of shape memory material having first and second anchoring zones and an intermediate zone. The prosthesis also includes graft material engaging at least a portion of the stent. During delivery of the prosthesis, the stent is in a substantially straight longitudinal configuration, and after delivery of the prosthesis the stent is returned to a coiled configuration. The diameter of the prosthesis may be adjusted by controlling the degree to which the stent is coiled.

Growing community of inventors

Miami Lakes, FL, United States of America

Kirk L Johnson