510(k) K071413 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
HEMICAP PATELLO-FEMORAL RESURFACING SYSTEM
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Nov 9, 2007 |
| Received | May 21, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071413
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.