510(k) K012800 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
| Applicant | Whiteside Biomechanics, Inc., Creve Coeur MO, US |
| Decision | Substantially Equivalent, May 3, 2002 |
| Received | Aug 21, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012800
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.