510(k) K014171 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
ADVANCE UNICONDYLAR KNEE SYSTEM
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Mar 15, 2002 |
| Received | Dec 20, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014171
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.