510(k) K130302 ยท MNI Orthosis, Spinal Pedicle Fixation
SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT
| Applicant | Spinevision S.A., Antony Cedex, FR |
| Decision | Substantially Equivalent, Jul 30, 2013 |
| Received | Feb 7, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130302
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.