510(k) K171789 ยท PHX Shoulder Prosthesis, Reverse Configuration
ARROW Reverse Porous Glenoid
| Applicant | Fournitures Hospitalieres Industrie, Quimper Finistere, FR |
| Decision | Substantially Equivalent, Jan 23, 2018 |
| Received | Jun 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171789
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.