510(k) K142980 ยท MRW System, Facet Screw Spinal Device
Proficient (TM) Facet Screw Spine System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jan 16, 2015 |
| Received | Oct 15, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142980
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.