510(k) K153356 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Spine Innovation Interbody System
| Applicant | Spine Innovation, LLC, Solana Beach CA, US |
| Decision | Substantially Equivalent, Jan 14, 2016 |
| Received | Nov 20, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153356
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.