510(k) K080411 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PLATEAU SPACER SYSTEM
| Applicant | Life Spine, Hoffman Estates IL, US |
| Decision | Substantially Equivalent, May 15, 2008 |
| Received | Feb 15, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080411
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.