510(k) K014072 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
FIXION UNIPOLAR MODULAR HEMI-HIP SYSTEM (FIXION UH)
| Applicant | Disc-O-Tech Medical Technologies, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 8, 2002 |
| Received | Dec 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014072
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.