510(k) K131522 ยท MNI Orthosis, Spinal Pedicle Fixation
CORE PEDICLE SCREW SYSTEM
| Applicant | Core-Nexus, Austin TX, US |
| Decision | Substantially Equivalent, Aug 9, 2013 |
| Received | May 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131522
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.