510(k) K203375 ยท PHX Shoulder Prosthesis, Reverse Configuration
OVOMotion Reverse Shoulder Arthroplasty System
| Applicant | Arthrosurface, Inc., Franklin ME, US |
| Decision | Substantially Equivalent, Jun 24, 2021 |
| Received | Nov 16, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203375
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.