510(k) K222015 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Integral Titanium Cervical Interbody
| Applicant | Nvision Biomedical Technologies, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Jul 5, 2023 |
| Received | Jul 8, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222015
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.