510(k) K160124 ยท MNI Orthosis, Spinal Pedicle Fixation
LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System
| Applicant | Spinevision S.A., Antony, FR |
| Decision | Substantially Equivalent, Apr 4, 2016 |
| Received | Jan 20, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160124
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.