Biomet Manufacturing Corporation

Encore Medical Corporation

Zimmer Gmbh

Biomet Sports Medicine, LLC

Limacorporate S.p.a.

Nathan A Winslow

John M McDaniel

Nicholas J Katrana

Clinton E Kehres

Thomas M Vanasse

Brian K Berelsman

Daniel Duane Fritzinger

Bryce Alan Isch

Kevin T Stone

Russell M Parrott

Michael Francis Kovacs

Benjamin Isaiah Joseph

Nicholas Muir

Gregory J Denham

Russell F Warren

Benjamin P Heilman

Michael A Wack

Jason M Hurst

Ben Joseph

Robert J Taylor

John W Sperling

Christopher M Palese

Joshua R Porter

Christopher Eash

Jeffrey Kneisl

Paul E Schwartz

Thomas J Graham

Daniel R Norton

Andrew K Palmer

Nicholas Michael Cordaro

H Gene Hawkins

Andrew Rolfe Hopkins

William Hartman

Hoang P Nguyen

Jason M Shultz

Aaron J Smits

Ravikumar Varadarajan

Kristen Martin

Andrew Matthew Telka

John Schulz

John M Mcdaniel

Kevin N Baird

Derek J Harper

Stephen H Hoag

Daniel Bryce Smith

David A Nolan

Donald H Lee

Edward V Craig

Lawrence Gulotta

Donald W Dye

Hill Hastings

Dean E Smeltzer

Robin Brown

Don Lee

Kane Wu

Michael Dziekan

Wolfgang Walter Vogt

Aaron Smits

Hoang Nguyen

Cordaro Nicholas M M

Stone Kevin T T

The present application relates to a tissue repair device that can include any one or combination of features including an end effector and an actuator. A deformable first anchor and a deformable second anchor can be captured by the end effector. The actuator can selectively engage the first anchor and the second anchor in a series. The actuator can deploy the first anchor from the end effector into tissue and then can be selectively moveable to engage and deploy the second anchor from the end effector into the tissue.

Repair device for deploying anchors into tissue

A method of soft tissue repair comprises attaching at least one suture to a soft tissue to be affixed to a bone structure, positioning a tissue anchor on a driver, positioning a cinching suture alongside the driver, engaging a catch of the cinching suture with a stop of the driver, capturing the at least one suture attached to the soft tissue in a loop of the cinching suture positioned proximate a distal tip of the driver, drawing the at least one suture toward the distal tip of the driver by pulling at least a first portion of the cinching suture; preventing the cinching suture from passing by the driver by engaging the catch with the stop, and installing the tissue anchor into the bone structure to secure the at least one suture in the bone structure by interference-friction fixation between the tissue anchor and the bone structure.

Knotless bone anchor system and method

Disclosed herein are suture systems and method of use thereof. The suture systems can include a passer, a needle, a first suture, and a second suture. The needle can be sized to pass through a cavity defined by the passer and define an attachment member. The first suture can include a first end, a second end, and a portion sized to be received by the attachment member and pass through the passer. The second suture can include a suture passage extending from a suture inlet to a suture exit. The first suture can be operable to pull a portion of the second suture at least partially around an anatomical structure. The second suture can be operable to reduce an anatomical structure when a first end of the second suture is passed through the suture passage.

Adjustable loop suture construct for joint repair

A glenoid implant is provided and may include a body portion and a stem portion. The stem portion may extend from the body portion along a longitudinal axis. The body portion may include an articular side and a bone-engaging side opposite the articular side. At least a portion of the bone-engaging side may be disposed at a non-parallel angle relative to at least a peripheral edge of the articulation side.

Glenoid implant

Disclosure herein are knotless suture anchor constructs and methods of use thereof. The suture anchor constructs can include a bone anchor and a suture. The bone anchor can include a suture anchoring member and can define a cavity and a longitudinal passage extending from a trailing end of the bone anchor at least partially therethrough to the cavity. The suture anchoring member can be located in the cavity. The suture can be coupled to the suture anchoring member and can include a tensioning portion, a repair portion, and an intermediate portion. The intermediate portion can form a suture loop extending along the longitudinal passage.

Suture anchor construct

A system for aligning components of a prosthetic includes a mounting plate, a fastener and an adapter coupling plate. The mounting plate comprises: a first major surface; a second major surface opposing the first major surface; an adapter accommodation hole extending through the mounting plate; and sizing indicia located on the second major surface. The fastener extends from the mounting plate. The adapter coupling plate comprises: a third major surface; a fourth major surface opposing the third major surface; an adapter coupling hole extending through the adapter coupling plate and surrounded by the adapter accommodation hole; and an indicator located on the fourth major surface to point to the sizing indicia on the mounting plate. The adapter coupling plate can be slidable along a slot surrounding the fastener or a tongue and groove system connecting the adapter coupling plate and the mounting plate and locked via the fastener.

Methods and apparatuses for trialing a humeral head

The disclosure includes methods and systems for making orthopedic connections where there is unique adjustability to the connection. Illustratively, one embodiment provides a connecting assembly for connecting a plurality of orthopedic components. Such connecting assemblies can include a first orthopedic component that provides a female bore. Additionally, the assembly can include a second orthopedic component that can be or include a male-type connecting member that is positionable in the bore of the first orthopedic component. In one preferred form, the male-type connecting member will be a quasi-spherical member. The quasi-spherical member can include a textured outer surface, e.g., for contacting one or more walls or surfaces in the bore in a fashion that removably locks or helps to removably lock or fix the quasi-spherical member in the bore.

Adjustable orthopedic connections

A humeral cut guide member for resectioning or resurfacing a humeral head, including a bone-engagement member including a first patient-specific bone-engagement surface that is complementary and made to substantially mate and nest in only one position on a specific patient's humeral head; a registration member connected to the bone-engagement member including a second patient-specific bone engagement surface that is sized and made to substantially mate and nest in only one position with the specific patient's bicipital groove; and a cut guide plate connected to the bone-engagement member and defining an elongated slot.

Patient-specific humeral guide designs

A self-adjusting suture construct can include a suture extending from a passive end to an active end. The passive end can include a first loop that the active end can be passed through to form a second loop. The active end can then be pulled to tighten the second loop around a portion of a patient's anatomy. The active end can be passed through an anchor and the anchor can be implanted to lock the tightened second loop.

Self-adjusting suture construct

A patient-specific guide tool for guiding an object toward a glenoid face of a scapula of a patient for implantation of a shoulder prosthetic device is disclosed. The guide tool includes a guide portion that includes a guide surface. The guide surface is configured to guide movement of the object toward the glenoid face. Furthermore, the guide tool includes a patient-specific portion that is operably coupled to the glenoid portion. The patient-specific portion includes at least one patient-specific surface that is three-dimensionally contoured and that is configured to nest and closely conform to a corresponding surface of the scapula to thereby position the guide surface at a predetermined position relative to the glenoid face.

Patient specific glenoid guide

A bone reamer includes a first member having a first hub and a second member having a second hub. The first hub can extend along a first axis and have a pair of elongated cutting arms that are fixed to the first hub. The elongated cutting arms can extend along a second axis that is generally perpendicular relative to the first axis. The first hub can define a track thereon. The second hub can extend along a third axis. The second member can have a second pair of elongated cutting arms that are fixed to the second hub and extend along a fourth axis that is generally perpendicular to the third axis. The second member can have a track follower extending thereon and that is configured to slidably advance along the track causing the first and second members to move between a collapsed position and an expanded position.

Glenoid reamer

A glenoid guide has an upper surface and a lower surface, wherein the lower surface is a patient-specific surface configured as a negative surface of a glenoid face based on a three-dimensional image of a shoulder joint of a patient reconstructed preoperatively from image scans of the shoulder joint of the patient. The glenoid guide includes an anatomic tubular drill guide extending from the upper surface along an anatomic alignment axis configured preoperatively with a patient-specific orientation and insertion location for guiding a glenoid implant into the glenoid face for anatomic shoulder arthroplasty. The glenoid guide includes a reverse tubular drill guide extending from the upper surface along a reverse alignment axis configured preoperatively with a patient-specific orientation and insertion location for guiding a glenoid baseplate into the glenoid face for reverse shoulder arthroplasty.

Patient-specific glenoid guides

Various parallax-free indicator devices, systems, and methods are disclosed. The indicator device may have a housing defining an aperture and a light source assembly at least partially disposed in the housing. The housing may be selectively securable via a fastener to an instrument in a selected orientation relative to the instrument. The light source assembly may have a light source operably coupled to a power source via a power circuit. The light source may be positioned within the housing to emit through the housing aperture. Upon activation, the light source assembly emits a parallax-free alignment indicator along an alignment axis that may have at least one of a selected angle and a selected displacement relative to a selected reference axis. The alignment indicator may guide a surgical procedure.

Parallax-free indicator devices, systems, and methods

A system for repairing a glenoid defect of a specific patient can include a patient-specific punch and a patient-specific shaping block. The patient-specific punch can form a patient-specific glenoid implant from a bone puck. The patient-specific shaping block can shape the patient-specific glenoid implant to match and fill a glenoid defect of a specific patient.

Patient specific reconstructive glenoid systems and methods

Growing community of inventors

Warsaw, IN, United States of America

Nathan A Winslow