510(k) K781735 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
ENDOPROSTHESIS SYSTEM, VARIO-HEAD
| Applicant | Waldemar Link GmbH & Co. KG, Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 24, 1978 |
| Received | Oct 12, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781735
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.