510(k) K926334 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
AXIOM TOTAL KNEE SYST/ACL RETAIN TIBIAL TRAY/INSER
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent for Some Indications, Oct 18, 1994 |
| Received | Dec 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926334
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.