510(k) K131393 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
MAK OSS FEMORAL KNEE COMPONENTS
| Applicant | Biomet Orthopedics Corp., Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 24, 2013 |
| Received | May 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131393
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.