510(k) K123297 ยท MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM
| Applicant | Biomet Manufactuting Corp., Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 20, 2012 |
| Received | Oct 22, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123297
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.