510(k) K121116 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PLATEAU SPACER SYSTEM
| Applicant | Life Spine, Hoffman Est IL, US |
| Decision | Substantially Equivalent, May 8, 2012 |
| Received | Apr 12, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121116
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.