510(k) K181799 · OWI Bone Fixation Cerclage, Sublaminar
ResCUBE Ligament Fixation System
| Applicant | Cousin Biotech Sas, Wervicq-Sud, FR |
| Decision | Substantially Equivalent, Aug 29, 2018 |
| Received | Jul 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181799
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.