510(k) K223181 ยท NKB Thoracolumbosacral Pedicle Screw System
NuVasive Reline System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jan 11, 2023 |
| Received | Oct 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223181
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.