510(k) K102293 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CALIBER SPACER
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Jan 5, 2011 |
| Received | Aug 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102293
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.