Cook Medical Technologies LLC

Muffin Incorporated

Charles Leland Baxter

Ryan C Bradway

Jarin A Kratzberg

Sara Marie Sherman

Neal E Fearnot

William John Havel

Keith Milner

Richard B Sisken

Kenneth Aaron Haselby

Richard Hadley

Blayne A Roeder

Steven Charlebois

Peter S McKinnis

James D Purdy

Zachary Wagner

Chantelle King

Stephan Haulon

Marc C Buhrmester

William J Bourdeau

James Thomas Jones

Benjamin Marchi

Zach Wagner

Kyle D Amick

Jennifer Rodenberg

Brandon Tran

Alexander Shrum

Peter S Mckinnis

Stephen Haulon

A handle assembly for a prosthesis delivery device is disclosed. The handle assembly comprises a stationary main handle having a proximal end and a distal end and an outer surface extending therebetween. A first helical groove is formed in at least a portion of the outer surface of the main handle and a first trigger wire actuation mechanism disposed about the main handle and rotatably moveable relative to the main handle. A first trigger wire is operatively connected to the first trigger wire actuation mechanism, the first trigger wire having a prosthesis capture condition and a prosthesis release condition. Movement of the first trigger wire actuation mechanism causes movement of the first trigger wire thereby moving the first trigger wire from the prosthesis capture condition to the prosthesis release condition. Additional trigger wire actuation mechanisms operatively connected to one or more additional trigger wires may also be disposed about the main handle.

Modular handle comprising a trigger wire actuation mechanism for a prosthesis delivery device

Disclosed herein is an anchor for use with a medical device. The anchor includes a coil, a barb, and a turn connecting the coil to the barb. The anchor may be made of a shape memory material. The coil may have a first handedness, and the turn may have a second handedness opposite the first handedness. The anchor may be attached to the medical device by a friction fit, in some cases without being attached by welding, soldering, adhesive, or crimping.

Spring barb for medical device

Prostheses and methods of making the same are provided. The prosthesis has an internal branch configuration. A trough or branch opening is at least partially defined by a trough wall extending into a main lumen from a sidewall of the prosthesis. The internal branch extends from the trough within the main lumen towards one of the outflow end of the graft body in a helical, retrograde arrangement. Other arrangements are described. The prosthesis may include a scalloped fenestration having a width larger than the trough. The trough may be positioned along a tapered region of the prosthesis. The trough and internal branch may be made from the same graft material. The trough and internal branch, in addition to the main graft body, may be made from the same graft material.

Prosthesis with side branch and method of making the same

A handle assembly for a prosthesis delivery device is described. The handle assembly comprises a stationary main handle having a proximal end and a distal end and an outer surface extending there between. A first handle extends proximally from the main handle and is rotationally moveable relative to the main handle, the first handle having a proximal end and a distal end and defining a first handle interior. A second handle extends distally from the main handle and is rotationally moveable relative to the main handle, the second handle having a proximal end and a distal end and defining a second handle interior. The first handle comprises a threaded internal surface extending between the proximal and distal ends and the second handle comprises a threaded internal surface extending between the proximal and distal ends.

Threaded modular handle for a prosthesis delivery device

A filling and sealing system is provided for efficiently filling a series of individual vials with therapeutic liquids. In particular embodiments, the system includes a filling zone or station, a sealing zone or station, an unloading zone or station, and electronic controls.

Systems and methods for filling and sealing vials

An endoluminal prosthesis assembly includes a delivery system having an introduction end, an operator end, and a stent graft retention region. An endoluminal prosthesis is disposed at the stent graft retention region. The prosthesis comprises a tubular body, an inner lumen extending between proximal and distal ends of the tubular body, at least one fenestration disposed in a sidewall of the body, and an internal branch at least partially formed with the sidewall of the body and disposed in parallel alignment with the prosthesis. A guide wire having a first end and a second end is pre-loaded with the prosthesis in the delivery system. At least a portion of the guide wire is disposed within the internal branch and the inner lumen of tubular body of the prosthesis prior to delivery of the prosthesis and during delivery and deployment of the prosthesis. The second end of the guide wire extends distally from the distal opening of the tubular body, and the first end of the guide wire extends through the internal branch and the at least one fenestration such that a portion of the guide wire is externally disposed relative to the prosthesis. The externally disposed portion of the guide wire is bent back on itself to form an externally disposed loop.

Preloaded branch wire loop constraint

A controlled expansion stent graft delivery system has an adjustment configuration in which a retractable sheath is at a retracted position out of contact with a stent graft, but expansion of the stent graft is controlled by a control tether, which has a middle segment wrapped around a fabric tube of the stent graft. The stent graft changes diameter responsive to a tension level in the control tether. At least one of an orientation and a position of the stent graft may be adjusted during controlled expansion via the control tether.

Controlled expansion stent graft delivery system

A needle disclosed herein may include an elongate body extending between a proximal end and a distal end with a central longitudinal axis defined by the body, where the distal end includes a single sharp point along the central longitudinal axis and defining a distal end terminus three longitudinal fluted surfaces converging at the distal end terminus; and three longitudinal beveled cutting edges defining borders between the fluted surfaces and converging at the distal end terminus. Needle embodiments may include one or more ports open into and/or proximal of the fluted surfaces and communicating with one or more longitudinal needle lumens.

Tri-fluted vascular access needle

A prosthesis delivery device includes an inner cannula, a positioner disposed coaxially over a first portion of the inner cannula, a concentric cannula disposed coaxially over a second portion of the inner cannula, and a tip assembly disposed over a third portion of the inner cannula. A distal end of the concentric cannula is attached to a proximal end of the positioner. The tip assembly comprises a distal tip segment and a proximal tip segment, with the distal tip segment attached to a proximal end of the concentric cannula and the proximal tip segment attached to a proximal end of the inner cannula. A prosthesis is carried on the concentric cannula and a sheath is mounted coaxially over the prosthesis. The sheath comprises a split defining a proximal sheath segment and a distal sheath segment. A proximal end of the proximal sheath segment is attached to the proximal tip segment.

Split sheath prosthesis deployment system with divided tip

A modular handle assembly for a prosthesis delivery device is disclosed. The modular handle assembly has a stationary main handle and a first handle that extends proximally from the main handle and is rotationally moveable relative to the main handle. A second handle extends distally from the main handle and is rotationally moveable relative to the main handle. The main handle has a first rotational interface and a second rotational interface that are configured to engage with the first handle and the second handle, respectively.

Modular handle for a prosthesis delivery device

Described in one aspect is a multi-cell or multi-chambered container for sealing various materials such as therapeutic or diagnostic agents, animal or human tissue, tissue samples, specimens, blood, genetic material, or any other material. The container includes seals formed by folding the wall of the elongate body transverse to the interior of the elongate body and maintaining the folded wall portions adjacent one another or joining them together. In another aspect, the container disclosed may be made according to a method involving creating multiple seals at various locations along the elongate body thus creating sealed voids or cells between the seals within the elongate body.

Multi-cell sealed container

A device for closure of an opening in a medical patient's blood vessel wall is disclosed. It discloses a plug shaft which is: porous; blood absorbing; insertable in an opening in a blood vessel wall; and, at least partially comprises an ECM material. A first cap which is integral with the plug shaft at a proximal end thereof is disclosed. A second cap is integral with the plug shaft. An insertion tube, a pusher, surgical methods of use, and kits, are also disclosed.

Degradable expanding closure plug

A dilation cap may include a distal tip, an intermediate body, and a proximal coupling member. The distal tip may at least partially surround a longitudinal axis of the dilation cap and may include a cavity to receive a distal end of a cannula of a medical device. The intermediate body may extend proximally from the distal tip and include a dilator portion. The dilator portion may include a projection extending laterally in a direction away from the longitudinal axis of the dilation cap. The proximal coupling member may extend proximally from the intermediate body and at least partially surround the longitudinal axis of the dilation cap. The proximal coupling member may be configured to engage an intermediate portion of the cannula of the medical device. The intermediate body may be asymmetrical with respect to the longitudinal axis of the dilation cap.

Growing community of inventors

West Lafayette, IN, United States of America

Charles Leland Baxter