510(k) K243191 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Atlas Spine Lateral Expandable Interbody System
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Nov 26, 2024 |
| Received | Sep 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243191
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.