510(k) K161798 · MRW System, Facet Screw Spinal Device
FacetBRIDGE® System
| Applicant | Ldr Spine USA, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Aug 4, 2016 |
| Received | Jun 30, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161798
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.