510(k) K062879 ยท MNI Orthosis, Spinal Pedicle Fixation
TRAVERSE OCT SPINAL FIXATION SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Dec 22, 2006 |
| Received | Sep 26, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062879
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.