510(k) K212050 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NGM WAVE PLIF Cage
| Applicant | NGMedical GmbH, Nonnweiler, DE |
| Decision | Substantially Equivalent, Dec 1, 2021 |
| Received | Jun 30, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212050
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.