510(k) K982389 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
ODC B2 BIPOLAR CUP
| Applicant | Ortho Development Corp., Draper UT, US |
| Decision | Substantially Equivalent, Oct 7, 1998 |
| Received | Jul 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982389
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.