510(k) K231099 ยท MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
SMR Hybrid Glenoid System
| Applicant | Lima Corporate S.P.A., Villanova Di San Daniele Del Friuli, IT |
| Decision | Substantially Equivalent, Dec 21, 2023 |
| Received | Apr 18, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231099
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.