510(k) K003363 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
M2A 32MM TAPER SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 15, 2000 |
| Received | Oct 27, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003363
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.