510(k) K173022 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SeaSpine Ventura NanoMetalene System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 26, 2017 |
| Received | Sep 28, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173022
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.