510(k) K233300 ยท NKB Thoracolumbosacral Pedicle Screw System
POWEReam 1/4 Drive
| Applicant | Stryker Instruments, Portage MI, US |
| Decision | Substantially Equivalent, Dec 26, 2023 |
| Received | Sep 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233300
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.