510(k) K180675 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Atlas Spine Expandable Cervical Interbody System
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Jun 13, 2018 |
| Received | Mar 15, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180675
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.