510(k) K173198 ยท MRW System, Facet Screw Spinal Device
Facet Screw Fixation System
| Applicant | U&I Corporation, Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Jan 3, 2018 |
| Received | Oct 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173198
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.