510(k) K193180 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Alliance Augmented Glenoid
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 24, 2020 |
| Received | Nov 18, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193180
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.