510(k) K130126 ยท MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 6, 2013 |
| Received | Jan 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130126
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.