510(k) K896853 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent for Some Indications, May 2, 1990 |
| Received | Dec 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896853
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.