510(k) K152200 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SurgTech Interbody System
| Applicant | Surgtech, Inc., Westlake OH, US |
| Decision | Substantially Equivalent, Mar 25, 2016 |
| Received | Aug 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152200
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.