Biomet Manufacturing Corporation

Synvasive Technology, Inc.

Midwest Training and Development Services, LLC

Florida Southern College

Keith R Berend

Robert G Metzger

Adolph V Lombardi

Michael E Berend

Ryan John Schoenefeld

Lance Dean Perry

Aaron P Smith

John Robert White

David Wycliffe Murray

Kirk J Bailey

Andrew P Sizelove

Michael G Fisher

David R Brown

Tyler D Witt

Andrew Freiberg

Hugh Apthorp

John Barrington

Christopher Peters

Stephanie Klunk

Jason D Meridew

Troy W Hershberger

Jacob Macke

Bradley T Durcholz

Christopher Eash

Austen Davenport

Daniel E Williamson

Shon David Steger

Radu Serban

Thomas Donaldson

Craig Della Valle

Jeffrey DeClaire

Zachary D Fralish

Shameka J Shelby

Christopher G Zochowski

Michael G Fischer

Brice Bedke

Brad Durcholz

Jeffrey Declaire

Lance D Perry

David Murray

Adolph Lombardi

A novel active agent-eluting hemostatic agent and methods of use and manufacture thereof are presented. A polymer, such as gelatin, is used as the base for a hemostatic agent. The gelatin is crosslinked with a chemical crosslinker, such as a carbodiimide, in the presence of an active agent. The active agent may be an anesthetic or antimicrobial, such as an antibiotic. The novel process allows for the active agent to be both covalently bound to the gelatin as well as be trapped within cages in the gelatin that are formed from the crosslinking. This dual measure allows for controlled and sustained release of the active agent from the hemostatic agent to reduce surgical site infections.

Active agent-eluting hemostatic agents for prevention of surgical site infection

An instrumentation set for preparing a proximal tibia during a bi-cruciate retaining procedure can include a tibial resection block and a stylus. The tibial resection block can be configured to be fixed to an anterior portion of the proximal tibia. The tibial resection block can define a slot that extends in a medial-lateral direction when the tibial resection block is fixed to the proximal tibia. The stylus can have a first block attachment feature and a second block attachment feature. The first block attachment feature can be offset from the stylus a first distance. The second block attachment feature can be offset from the stylus a second distance. The first and second block attachment features of the stylus can be selectively and alternatively received by the slot of the tibial resection block to position the stylus at distinct offset locations relative to the slot.

Bi-cruciate knee system

A method of preparing a knee joint for a prosthesis in a patient includes mating a patient-specific three-dimensional curved inner surface of a femoral alignment guide onto a corresponding three-dimensional femoral joint surface of the patient. The patient-specific three-dimensional curved inner surface is preoperatively configured from medical scans of the knee joint of the patient. First and second holes are drilled into an anterior portion of the femoral joint surface through corresponding first and second guiding apertures of the femoral alignment guide.

Patient-specific knee alignment guide and associated method

The present disclosure relates generally to the field of medical treatment and therapy of mammalian tissue. More specifically, it relates to coverings and/or dressings that provide negative pressure at mammalian tissue sites, such as at one or more sites of surgical, non-surgical, and/or traumatic wounds, to promote closure and healing of the wounds. A key embodiment of the disclosed invention entails the use of a dressing that comprises a sponge that is shaped so as to create a vector force inward bringing wound edges together to promote healing, especially upon application of negative pressure. Other key features of the disclosed invention are its simplicity, its low cost, and that it is completely mechanical and lacks the need for any electronic components. The disclosure also relates to devices, systems, kits and methods for providing said negative pressure at said mammalian tissue sites and promote healing.

Negative pressure wound apposition dressing system

A method of preparing a surgical plan comprises video capturing a range of motion of an anatomic joint of a patient to obtain a range of motion video, registering the range of motion video to two-dimensional images of a skeleton of the patient, identifying potential impingement and stability issues in the anatomic joint based on the range of motion video, templating a prosthetic implant on two-dimensional images of the anatomic joint using the identified potential impingement and stability issues of the anatomic joint to obtain position and orientation data, and electronically saving the position and orientation data of the prosthetic implant for use with a surgical navigation system. A system for planning and performing a surgical procedure comprises a motion capture system, an x-ray system, an electronic modeling system, and a surgical navigation system.

Method and system for planning and performing arthroplasty procedures using motion-capture data

An alignment plate can be designed and formed based upon a known geometry of a subject, such as a human patient. The alignment plate can include various members, such as a plurality of fingers or legs, to contact the selected points of the anatomy. Based upon contact of the fingers at the selected points of the anatomy, the alignment plate can be aligned at a preselected or predetermined alignment with a portion of the anatomy, such as an acetabulum.

Subject contacting plate

An acetabular prosthesis is described that includes a shell having an outer surface and an inner surface, the outer surface defining an external shape. There is at least one through bore extending from the outer surface of the shell to the inner surface of the shell. At least one augment is configured to be positioned at least partially within the at least one through bore of the shell such that, in an assembled state, the shell and the at least one augment define a modified external shape.

Threaded augmentable acetabular shell with augments

A method of securing an orthopedic hip prosthesis to an acetabulum of a living being. The prosthesis can be a shell or a cup, and the surgery can be a total hip arthroplasty such as a revision total hip arthroplasty. In some examples the method can include placing an augment at a bone surface of the acetabulum, applying a layer of fixation material over the bone surface in an amount sufficient to cover the augment, and then implanting the prosthesis over the layer of fixation material to secure the prosthesis to the layer of fixation material. In various aspects of the method, the augment can be an anchor or a spacer.

Augments and methods for implanting hip prostheses

An implant for a hip can include a lateral augment adapted to be coupled to a lateral side of a femoral body implant. The lateral augment can include a body portion having a first surface, a second surface opposite the first surface, and a protrusion extending from the second surface. The protrusion can have a shape adapted to mate with a complementary shaped recess formed in the lateral side of the femoral body implant. An aperture can be positioned in the body portion and extend through the protrusion. A fastener can be received through the aperture and adapted to be threadably secured to the lateral bore. The fastener can be configured to have a length sufficient to pass through a portion of a greater trochanter for securing the portion of the greater trochanter and the lateral augment to the femoral body implant.

Modular lateral hip augments

Systems, devices, and methods are provided for measuring forces in the space of a knee during surgery. Such forces can be caused by tension in the ligaments of the knee. A femoral member is engaged with a distal femur. While the knee is flexed, partially extended, or fully extended, a force sensor and a gauge shim can be placed in the gap between the femoral member and the tibial plateau to measure the forces therebetween. The force sensor provides an accurate and quantifiable measurement of force, making knee replacement surgery and ligament tension balancing more accurate, standardized and repeatable. The force sensor comprises an elongate housing which comprises a thin force sensing distal portion and a proximal handle portion.

Sensing force during partial or total knee replacement surgery

An orthopedic implant includes a first portion including at least one feature modified to be patient-specific and match the anatomy of a specific patient from a three-dimensional digital image of a patient's joint using computer modeling. The orthopedic implant includes a non-custom inner bone-engaging surface including a plurality of planar surfaces configured for engagement with non-custom bone cuts.

Patient-modified implant

Sensing force during partial and total knee replacement surgery

Growing community of inventors

Columbus, OH, United States of America

Keith R Berend