510(k) K180891 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EVOL Spinal Interbody System, EVOS Lumbar Interbody System
| Applicant | Cutting Edge Spine, LLC, Waxhaw NC, US |
| Decision | Substantially Equivalent, May 4, 2018 |
| Received | Apr 5, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180891
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.