510(k) K180729 ยท MRW System, Facet Screw Spinal Device
FaSet Fixation System
| Applicant | Huvexel Co. , Ltd., Seongnam-Si, KR |
| Decision | Substantially Equivalent, Jun 28, 2018 |
| Received | Mar 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180729
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.