510(k) K060127 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
HEMICAP PATELLO-FEMORAL RESURFACING PROSTHESIS
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Mar 16, 2006 |
| Received | Jan 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060127
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.