510(k) K233919 ยท HRS Plate, Fixation, Bone
VariAx 2 Distal Radius System
| Applicant | Stryker GmbH, Selzach, Solothurn, Ch, CH |
| Decision | Substantially Equivalent, Mar 25, 2024 |
| Received | Dec 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233919
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.