510(k) K012762 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
MJS POSTERIOR STABILIZED KNEE SYSTEM
| Applicant | Osteoimplant Technology, Inc., Hunt Valley MD, US |
| Decision | Substantially Equivalent, Dec 11, 2001 |
| Received | Aug 17, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012762
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.