510(k) K150410 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
RESTORIS POROUS PARTIAL KNEE SYSTEM
| Applicant | Mako Surgical Corporation, Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Mar 20, 2015 |
| Received | Feb 18, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150410
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.