510(k) K163506 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Coalesce (-Straight, -Convex, -Crescent, -Lateral, -Anterior, or -Oblique) Lumbar Interbody Fusion System
| Applicant | Vertera, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Jun 19, 2017 |
| Received | Dec 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163506
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.