510(k) K061433 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 21, 2006 |
| Received | May 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061433
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.