510(k) K011509 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
BARRETT UNICONDYLAR TIBIAL BEARING
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 13, 2001 |
| Received | May 16, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011509
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.