510(k) K112607 ยท NKB Thoracolumbosacral Pedicle Screw System
SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ...
| Applicant | Spinevision S.A., Douglassville PA, US |
| Decision | Substantially Equivalent, Jun 7, 2012 |
| Received | Sep 7, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112607
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.