510(k) K191960 ยท PHX Shoulder Prosthesis, Reverse Configuration
Arthrex Univers Revers Modular Glenoid System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Dec 23, 2019 |
| Received | Jul 23, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191960
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.