510(k) K082088 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM II
| Applicant | Mako Surgical Corp., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Oct 22, 2008 |
| Received | Jul 24, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082088
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.