510(k) K132412 ยท MNI Orthosis, Spinal Pedicle Fixation
INERTIA MIS PEDICLE SCREW SYSTEM
| Applicant | Nexxt Spine, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Oct 10, 2013 |
| Received | Aug 2, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132412
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.