510(k) K192497 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EVOL ha - D Lateral Interbody Fusion System
| Applicant | Cutting Edge Spine, LLC, Waxhaw NC, US |
| Decision | Substantially Equivalent, Jan 6, 2020 |
| Received | Sep 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192497
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.