510(k) K120353 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
SYNSTER PEDICLE SCREW SYSTEM SYNSTER PLUS PEDICLE SCREW SYSTEM
| Applicant | Bm Korea Co., Ltd., Fullerton CA, US |
| Decision | Substantially Equivalent, May 9, 2012 |
| Received | Feb 6, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120353
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.