510(k) K133575 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
SPINEVISION LUMIS CANNULATED PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. PEDICLE SCREW FIXATION SYSTEM
| Applicant | Spinevision S.A., Antony Cedex, FR |
| Decision | Substantially Equivalent, Jun 30, 2014 |
| Received | Nov 20, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133575
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.