510(k) K231658 ยท NKB Thoracolumbosacral Pedicle Screw System
VEOS Spinal Fixation System
| Applicant | Spineway, Ecully, FR |
| Decision | Substantially Equivalent, Oct 10, 2023 |
| Received | Jun 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231658
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.