510(k) K254017 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SWINGO-3D Lumbar Cage System
| Applicant | Implanet, Allee Francois Magendie, FR |
| Decision | Substantially Equivalent, Feb 26, 2026 |
| Received | Dec 15, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K254017
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.