510(k) K073531 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
ACCIN PEDICLE SCREW SYSTEM
| Applicant | Accelerated Innovation, LLC, Clifton NJ, US |
| Decision | Substantially Equivalent, Feb 4, 2008 |
| Received | Dec 17, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073531
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.