510(k) K143192 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Vanguard 360 Revision Knee System
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 12, 2015 |
| Received | Nov 6, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143192
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.