510(k) K142488 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura) NanoMetalene, Cambria NanoMetalene , Vu aPOD-L NanoMetalene, Vu ePOD NanoMetalene
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Dec 18, 2014 |
| Received | Sep 4, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142488
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.