510(k) K261683 ยท PHX Shoulder Prosthesis, Reverse Configuration
Augment Off-Axis Instrument System
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 16, 2026 |
| Received | May 21, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261683
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.