510(k) K112986 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LATERAL FUSION DEVICE
| Applicant | Integra Spine (Integra Lifesciences), Medina OH, US |
| Decision | Substantially Equivalent, May 1, 2012 |
| Received | Oct 6, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112986
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.