5510-F-101
Stryker Triathlon CR Femoral Component, #1 Left Cemented
$11.50
box of 1
Out of stock
Expiration:
Expired
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The item listed above is expired and may be used for educational, training, and non-clinical research purposes only. Any product information appearing below, including the product indication statement, pertains to an in-date item only.
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Description
Stryker Orthopedics Triathlon Total Knee Replacement System
Implants
The Triathlon Knee System is designed to meet patients’ expectations for Lifestyle Recovery. The intuitive and evolutionary design is predicated on the worldwide clinical success of millions of Stryker knee implantations. The Triathlon Knee System is designed to provide patients more natural motion and the potential for greater implant longevity.
The Triathlon Knee is an evolutionary design developed to more closely reproduce natural knee motion, designed to provide mobility with stability through 150+ degrees of flexion.
Instruments
The Triathlon Knee System Instrumentation has been developed based on Stryker’s 30 year orthopaedic history. The system combines the engineering expertise of Human Factors Engineers with the experience of surgeons and OR staff worldwide. The Triathlon Knee System Instrumentation provides optimal OR efficiency and intra-operative flexibility through an Orthonomic design.
Additional information
| Size | 1 |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | box of 1 |
- FDA Product Code: JWH MBH
- FDA Product Code Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer / Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
- GMDN Term Code: 32831
- GMDN Term Name: Uncoated knee femur prosthesis, metallic
- GMDN Term Description: An implantable device designed to replace the femoral condyles (femoral component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint and its implantation is intended to be performed with bone cement.
