510(k) K183172 ยท HRS Plate, Fixation, Bone
Stryker SternalPlate System
| Applicant | Stryker, Portage MI, US |
| Decision | Substantially Equivalent, Mar 5, 2019 |
| Received | Nov 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183172
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.