510(k) K172371 ยท PHX Shoulder Prosthesis, Reverse Configuration
Arthrex UNIVERS REVERS COATED BASEPLATE
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 22, 2018 |
| Received | Aug 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172371
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.