510(k) K152137 ยท MRW System, Facet Screw Spinal Device
FacetBRIDGE System
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Jan 25, 2016 |
| Received | Jul 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152137
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.