510(k) K221048 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
Episealer Patellofemoral System
| Applicant | Episurf Medical, Inc., New York NY, US |
| Decision | Substantially Equivalent, Dec 23, 2022 |
| Received | Apr 8, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221048
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.