510(k) K162918 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Atlas Spine Expandable Interbody System
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Feb 9, 2017 |
| Received | Oct 18, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162918
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.