510(k) K922864 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
MUELLER TYPE FEMORAL STEM
| Applicant | Osteo Technology, Inc., Timonium MD, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | Jun 4, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922864
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.