510(k) K011810 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
ORTHOGENESIS LPS PROXIMAL TIBIAL REPLACEMENT AND ORTHOGENESIS LPS TIBIAL BEARING
| Applicant | Depuy, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 7, 2001 |
| Received | Jun 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011810
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.