510(k) K884837 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
KINEMAX TIBIAL WEDGE
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Feb 17, 1989 |
| Received | Nov 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884837
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.