510(k) K173260 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SeaSpine Spacer System (NanoMetalene)- Hollywood, Hollywood VI, Ventura, Pacifica; SeaSpine Spacer System -Hollywood, Hollywood VI, Ventura, Pacifica; SeaSpine Vu e·POD System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Dec 4, 2017 |
| Received | Oct 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173260
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.