510(k) K151665 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SUSTAIN Additional Implants
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Mar 16, 2016 |
| Received | Jun 19, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151665
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.