510(k) K200171 ยท PHX Shoulder Prosthesis, Reverse Configuration
SMR TT Augmented Glenoid System
| Applicant | Lima Corporate S.P.A., Villanova Di San Daniele Del Friuli, IT |
| Decision | Substantially Equivalent, Nov 19, 2020 |
| Received | Jan 23, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200171
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.