510(k) K150223 ยท MRW System, Facet Screw Spinal Device
Facet-Link Stabilization Platform
| Applicant | Facet-Link, Inc., Rockaway NJ, US |
| Decision | Substantially Equivalent, Apr 28, 2015 |
| Received | Jan 30, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150223
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.