510(k) K994184 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
PLR SPLINED REVISION STEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 15, 2000 |
| Received | Dec 10, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994184
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.