510(k) K884889 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
| Applicant | Protek, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 27, 1989 |
| Received | Nov 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884889
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.