510(k) K191810 ยท NKB Thoracolumbosacral Pedicle Screw System
Curiteva Pedicle Screw System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Aug 28, 2019 |
| Received | Jul 5, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191810
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.