510(k) K162426 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
nva, nvp, and nvt
| Applicant | Nvision Biomedical Technologies, LLC, San Antonio TX, US |
| Decision | Substantially Equivalent, Sep 29, 2016 |
| Received | Aug 30, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162426
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.