510(k) K231743 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and Oro Lateral Plate System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 8, 2023 |
| Received | Jun 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231743
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.