510(k) K020291 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
EXACTECH, MODEL PMMA FEMORAL STEM CENTRALIZER
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Feb 27, 2002 |
| Received | Jan 28, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020291
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.