510(k) K123932 ยท MRW System, Facet Screw Spinal Device
ZYGAFIX SPINAL FACET SCREW SYSTEM
| Applicant | X-Spine Systems, Inc., Miamisburg OH, US |
| Decision | Substantially Equivalent, May 1, 2013 |
| Received | Dec 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123932
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.