510(k) K120340 ยท MRW System, Facet Screw Spinal Device
VENUS FACET SCREW SYSTEM
| Applicant | Apollo Spine, Inc., Stoughton MA, US |
| Decision | Substantially Equivalent, Oct 19, 2012 |
| Received | Feb 3, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120340
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.