510(k) K121850 ยท MRW System, Facet Screw Spinal Device
Typhoon(TM) Facet Screw Fixation System
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, Sep 20, 2012 |
| Received | Jun 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121850
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.