510(k) K240368 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
E3D-A Interbody System
| Applicant | Evolution Spine, Dallas TX, US |
| Decision | Substantially Equivalent, May 15, 2024 |
| Received | Feb 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240368
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.