510(k) K072336 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
REGENEREX POROUS TITANIUM SLEEVE AUGMENTS
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 5, 2007 |
| Received | Aug 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072336
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.