510(k) K090952 ยท MRW System, Facet Screw Spinal Device
ZYFUSE FACET FIXATION SYSTEM
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Jul 14, 2009 |
| Received | Apr 3, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090952
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.