510(k) K260102 ยท PHX Shoulder Prosthesis, Reverse Configuration
Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System
| Applicant | Stryker Corporation (Tornier, Inc.), Bloomington MN, US |
| Decision | Substantially Equivalent, Jun 12, 2026 |
| Received | Jan 13, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260102
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.