510(k) K212477 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EARP Interbody System
| Applicant | Nvision Biomedical Technologies, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Apr 28, 2022 |
| Received | Aug 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212477
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.