510(k) K101815 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
ENDURO KNEE SYSTEM
| Applicant | Aesculap Implant Systems, Center Valley PA, US |
| Decision | Substantially Equivalent, Dec 20, 2010 |
| Received | Jun 30, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101815
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.