510(k) K172206 · OWI Bone Fixation Cerclage, Sublaminar
NAJA Ligament Correction System
| Applicant | Cousin Biotech Sas, Wervicq-Sud, FR |
| Decision | Substantially Equivalent, Apr 10, 2018 |
| Received | Jul 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172206
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.