510(k) K200552 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EVOS Lumbar Interbody System
| Applicant | Cutting Edge Spine, LLC, Waxhaw NC, US |
| Decision | Substantially Equivalent, Apr 2, 2020 |
| Received | Mar 3, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K200552
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.