510(k) K121172 ยท MNI Orthosis, Spinal Pedicle Fixation
REFORM PEDICLE SCREW SYSTEM
| Applicant | Spinal USA, Pear MS, US |
| Decision | Substantially Equivalent, Aug 8, 2012 |
| Received | Apr 17, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121172
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.