510(k) K190636 · NKB Thoracolumbosacral Pedicle Screw System
NuVasive® Reline® 4.5-5.0 System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 19, 2019 |
| Received | Mar 12, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190636
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.