Device Dossier
JOURNEY II BCS OXINIUM Femoral Component - Uncoated knee femur prosthesis
Device Dossier for JOURNEY II BCS OXINIUM Femoral Component - Uncoated knee femur prosthesis (Uncoated knee femur prosthesis, Class III, sponsor Smith &…
- GMDN category: Uncoated knee femur prosthesis
- Sponsor: Smith & Nephew
Intended purpose
The JOURNEY II BCS Knee System is indicated for rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis; failed osteotomies, unicompartmental replacement, or total knee replacement. Posterior stabilized knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact. Constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are incompetent. The device is indicated for use only in surgeries where the patella is resurfaced.
Functional description
A sterile implantable device designed to replace the femoral condyles of the knee joint. The device articulates with tibial inserts, and patellar prosthetic components of the knee joint.