510(k) K222381 · HRS Plate, Fixation, Bone
PeriPRO Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System
| Applicant | Stryker GmbH, Mahwah NJ, US |
| Decision | Substantially Equivalent, Apr 27, 2023 |
| Received | Aug 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222381
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.