Vanguard Knee Posterior Stabilised Interlok closed box femoral component - Uncoated knee femur prosthesis

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

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:

Posterior stabilised Interlok finish femoral component for use in total knee arthroplasty. Accommodates distal and posterior augment options, with closed box design This component must be used with a tibial tray component and one of 2 posterior stabilized bearing options. Chrome/cobalt/molybdenum alloy Interlok finish closed box femoral component for use in knee joint replacement due to 1) painful, and disabled joint resulting from avascular necrosis, arthritis (all types) 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 posterior stabilised femoral component is designed for use where the posterior cruciate ligament requires substitution. The Interlok finish is designed for use with bone cement.

Authorization status:

A

Authorization date:

2013-12-18