510(k) K142218 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Coalition AGX Plate and Coalition AGX Spacer
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Mar 31, 2015 |
| Received | Aug 12, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142218
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.