510(k) K230219 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Eminent Spine 3D Lumbar Interbody Fusion Systems
| Applicant | Eminent Spine, LLC, Plano TX, US |
| Decision | Substantially Equivalent, May 16, 2023 |
| Received | Jan 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230219
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.