510(k) K070933 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
LOWTOP PEDICLE SCREW SYSTEM
| Applicant | Sanacor, American Fork UT, US |
| Decision | Substantially Equivalent, Jun 13, 2007 |
| Received | Apr 3, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070933
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.