510(k) K150321 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EVOS Lumbar Interbody System
| Applicant | Cutting Edge Spine, LLC, Waxhaw NC, US |
| Decision | Substantially Equivalent, Jul 13, 2015 |
| Received | Feb 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150321
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.