510(k) K142499 ยท NKB Thoracolumbosacral Pedicle Screw System
Reline System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 19, 2014 |
| Received | Sep 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142499
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.