Overview
This post-market clinical follow-up study intends to investigate long-term functionality of the VEGA System®. The design of the VEGA System® is meant to provide the patient with more knee mobility compared to their pre-operative state.The endpoint is the revision of at least one of the prosthesis components
Eligibility
Inclusion Criteria
- Patient from 18 to 75 years old
- Patient is able to comply with follow-up requirements including postoperative self-evaluations.
- Patient requires a primary knee replacement.
- Patient has a diagnosis of osteoarthritis
- Patient has intact collateral ligaments.
Exclusion Criteria
- Vulnerable patient under legal protection
- Patients with inflammatory arthritis.
- Patients that have had a high tibial osteotomy or femoral osteotomy.
- Pregnancy