510(k) K080330 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
SEGMENTAL DISTAL FEMORAL COMPONENTS AND PROXIMAL FEMORAL BODIES WITH A COMPRESS FEMALE TAPER
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 11, 2008 |
| Received | Feb 6, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080330
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.