Vanguard Knee Cruciate Retaining Interlok Femoral component - Uncoated knee femur prosthesis

Available from:

Zimmer Biomet Pty Ltd

Class:

Class III

Manufactured by:

Biomet Orthopedics 56 East Bell Drive, Warsaw, IN, 46581 United States Of America

Therapeutic area:

32831 - Uncoated knee femur prosthesis

Therapeutic indications:

Cruciate retaining Interlok finish femoral component for use in total knee arthroplasty. The CR femoral component has removable lugs to allow for posterior and distal augment options. This component must be used with a tibial tray component and one of 3 cruciate retaining bearing options. Chrome/cobalt/molybdenum alloy cruciate retaining femoral component for use in knee joint replacement due to 1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved 2) correction of varus, valgus, or posttraumatic deformity 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure The Interlok finish is designed for use with bone cement.

Authorization status:

A

Authorization date:

2013-12-13