510(k) K060303 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
VANGUARD PS OPEN BOX POROUS FEMORAL COMPONENTS
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 30, 2006 |
| Received | Feb 6, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060303
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.