510(k) K193645 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
nva, nvp, and nvt
| Applicant | Nvision Biomedical Technologies, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Jan 13, 2020 |
| Received | Dec 30, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K193645
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.