510(k) K222415 ยท NKB Thoracolumbosacral Pedicle Screw System
Rexious Spinal Fixation System
| Applicant | Dio Medical Corporation, East Norriton PA, US |
| Decision | Substantially Equivalent, Oct 25, 2022 |
| Received | Aug 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222415
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.