510(k) K182039 ยท PHX Shoulder Prosthesis, Reverse Configuration
Arthrex Univers Revers Porous Coated Baseplate and Universal Glenoid Inlay
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 28, 2018 |
| Received | Jul 30, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182039
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.