510(k) K061041 ยท MRW System, Facet Screw Spinal Device
US SPINE FACET FIXATION SYSTEM
| Applicant | Us Spine, Apple Valley MN, US |
| Decision | Substantially Equivalent, Jun 19, 2006 |
| Received | Apr 14, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061041
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.