510(k) K171832 ยท NKB Thoracolumbosacral Pedicle Screw System
Range/Denali/Mesa Spinal System
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Sep 14, 2017 |
| Received | Jun 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171832
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.