510(k) K121149 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
VANGUARD SSK 360 REVISION KNEE SYSTEM
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, May 16, 2012 |
| Received | Apr 16, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121149
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.