510(k) K261067 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BEE PLIF Cage
| Applicant | NGMedical GmbH, Nonnweiler, DE |
| Decision | Substantially Equivalent, Apr 30, 2026 |
| Received | Apr 1, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261067
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.