510(k) K142594 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
nva, nvp, nvt
| Applicant | Nvision Biomedical Technologies, LLC, San Antonio TN, US |
| Decision | Substantially Equivalent, Nov 28, 2014 |
| Received | Sep 15, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142594
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.