510(k) K172350 ยท HRS Plate, Fixation, Bone
AxSOS 3 Ti
| Applicant | Stryker GmbH, Selzach, Solothurn, Ch, CH |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Aug 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172350
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.