510(k) K083567 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW
| Applicant | Co-Ligne AG, Concord CA, US |
| Decision | Substantially Equivalent, Sep 14, 2009 |
| Received | Dec 3, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083567
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.