510(k) K133811 ยท NJD Prosthesis, Knee, Femorotibial, Unicompartmental/Unicondylar, Uncemented, Porous-Coated, Metal/Polymer
RESTORIS POROUS PARTIAL KNEE SYSTEM
| Applicant | Mako Surgical Corp., New York NY, US |
| Decision | Substantially Equivalent, Jul 8, 2014 |
| Received | Dec 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133811
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.