510(k) K060412 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
ACTIVE UNICOMPARTMENTAL KNEE SYSTEM
| Applicant | Australian Surgical Design & Manufacture, Annapolis MD, US |
| Decision | Substantially Equivalent, May 17, 2006 |
| Received | Feb 16, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060412
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.