Biomet Sports Medicine, LLC

Cook Medical Technologies LLC

Biomet Manufacturing Corporation

King Systems Corporation

Zachary Wagner

Kevin T Stone

Gregory J Denham

Blayne A Roeder

Brian K Berelsman

William John Havel

Jarin A Kratzberg

Siddharth Vad

Bryan Eliot Rolfs

Michael P DeBruyne

Rick Hadley

Tony C Hopkins

Charles Leland Baxter

Thomas W McGrail

Andrew P Isch

Yun Siung Tony Yeh

Matt Streicher

Paul Weidling

Michael P Debruyne

Amy Hruska

Caleb Coburn

Siddarth Vad

Michael Debruyne

An apparatus can include a first flexible member having first and second ends and a first body extending therebetween, where the first body defines a first passage portion. A second flexible member can have first and second ends and a second body extending therebetween, where the second body defines second and third passage portions. The first end of the first flexible member passes into and through the second passage portion such that the first end extends outside of the second passage portion, and the second end of the first flexible member passes into and through the third passage portion such that the second end extends outside of the third passage portion. The first and second ends of the second flexible member pass into and through the first passage portion to form a self-locking adjustable flexible member construct.

Method and apparatus for forming a self-locking adjustable loop

An apparatus can include a first flexible member having first and second ends and a first body extending therebetween that defines a first passage portion. A second flexible member can include first and second ends and a second body extending therebetween that defines a second passage portion. The first end of the first flexible member can pass into and through the second passage portion in a first direction such that the first end extends outside of the second passage portion. The first end of the second flexible member can pass into and through the first passage portion in a second direction such that the first end of the second flexible member extends outside of the first passage portion to form a self-locking adjustable flexible member construct. Applying tension to the first ends can draw the passage portions and corresponding second ends toward each other.

The present embodiments provide systems and methods for deploying at least a portion of a stent. In one embodiment, the system comprises a cannula having an outer surface, and at least one coiled member having proximal and distal ends and a plurality of turns disposed therebetween. One of the proximal and distal ends of the coiled member is secured to the outer surface of the cannula, and the other of the proximal and distal ends of the coiled member is unsecured relative to the outer surface of the cannula. A portion of a stent is looped around the unsecured end of the coiled member and disposed within spacing between adjacent turns of the coiled member. Rotation of the cannula subsequently causes the portion of the stent to disengage from the coiled member.

Systems and methods for deploying a portion of a stent using at least one coiled member

A method and apparatus for securing a fractured or sectioned sternum in a patient's body is disclosed. The apparatus can include an attachment member and an adjustable flexible member construct. The attachment member can have a flexible member holder. The adjustable flexible member construct can have first and second ends and a body defining at least one passage portion. The first and second ends can be passed into and through the at least one passage portion via first and second openings associated with the at least one passage portion of the adjustable flexible member construct to form a pair of loops. The attachment member can be configured to be coupled to at least one of the formed pair of loops. The adjustable flexible member construct can be positioned about the sternum and can be reduced to compress the fractured or sectioned sternum.

Method and apparatus for sternal closure

Method and Apparatus for Sternal Closure

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.

Dilation cap for endoluminal device

A method and tool for forming a hole in a bone. The method includes bringing a bone cutting tool extending along a longitudinal axis into engagement with a cortical portion of the bone. A distal portion of the bone cutting tool is passed into the cortical portion of the bone up to a first predetermined depth to form a first bore. The bone cutting tool is then driven in the axial direction to a second predetermined depth to form a keyway portion in the first bore with a cutting tooth of the bone cutting tool. The bone cutting tool is then rotated about the longitudinal axis to form a second bore in a cancellous portion of the bone. The first bore and the second bore have a shoulder extending therebetween. The bone cutting tool is removed from the hole formed by the first and second bores in the bone.

Method and apparatus for forming a hole in bone during a surgical procedure

The present embodiments provide systems and methods for deploying at least a portion of a stent. In one embodiment, the system comprises a cannula having an outer surface, and a coiled member having proximal and distal ends and a plurality of turns disposed therebetween. At least a portion of the coiled member is secured to the outer surface of the cannula. A stent is releasably secured to a portion of the coiled member. A protective cage may encircle the coiled member.

Growing community of inventors

Noblesville, IN, United States of America

Zachary Wagner