510(k) K162715 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SeaSpine Spacer System- Hollywood NanoMetalene, Hollywood VI NanoMetalene, Ventura NanoMetalene; SeaSpine Cambria NanoMetalene
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 28, 2016 |
| Received | Sep 29, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162715
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.