510(k) K140883 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
VANGUARD 360 OSSEOTI TIBIAL SLEEVE AUGMENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 30, 2014 |
| Received | Apr 7, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140883
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.