510(k) K243739 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AxCess® Expandable Interbody System
| Applicant | Elliquence, LLC, Baldwin NY, US |
| Decision | Substantially Equivalent, Jan 24, 2025 |
| Received | Dec 4, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243739
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.