510(k) K984296 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 18, 1999 |
| Received | Dec 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984296
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.