510(k) K231253 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
Overture Orthopaedics Patellofemoral System
| Applicant | Overture Resurfacing, Inc., New York NY, US |
| Decision | Substantially Equivalent, Jul 7, 2023 |
| Received | May 1, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231253
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.