510(k) K862460 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
FEMORAL HEMI-HIP PROSTHESIS
| Applicant | Orthopaedic Device Corp., Paterson NJ, US |
| Decision | Substantially Equivalent, Oct 6, 1986 |
| Received | Jun 30, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862460
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.