510(k) K121551 ยท MRW System, Facet Screw Spinal Device
RESOLUTE FACET SCREW SYSTEM
| Applicant | Neurostructures, LLC, Colorado Springs CO, US |
| Decision | Substantially Equivalent, Oct 23, 2012 |
| Received | May 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121551
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.