510(k) K082081 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
MAKO SURGICAL CORPORATION UNICONDYLAR KNEE IMPLANT SYSTEM III
| Applicant | Mako Surgical Corp., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Oct 15, 2008 |
| Received | Jul 23, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082081
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.