510(k) K143683 ยท NKB Thoracolumbosacral Pedicle Screw System
APEX-DL Spine System
| Applicant | Spinecraft, LLC, Westmont IL, US |
| Decision | Substantially Equivalent, May 22, 2015 |
| Received | Dec 24, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143683
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.