510(k) K150417 ยท NKB Thoracolumbosacral Pedicle Screw System
ASTRA SPINE SYSTEM
| Applicant | Spinecraft, LLC, Westmont IL, US |
| Decision | Substantially Equivalent, May 19, 2015 |
| Received | Feb 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150417
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.