510(k) K183553 ยท MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
Compress and Mini Compress Anti-Rotation Spindles
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 22, 2019 |
| Received | Dec 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183553
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.