510(k) K173900 ยท PHX Shoulder Prosthesis, Reverse Configuration
Arthrex Univers Revers Modular Glenoid System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Apr 20, 2018 |
| Received | Dec 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173900
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.