510(k) K162693 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VertebraLINK Fusion Platform
| Applicant | Facetlink Dba Linkspine, Rockaway NJ, US |
| Decision | Substantially Equivalent, Mar 29, 2017 |
| Received | Sep 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162693
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.