510(k) K083894 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ALIF SPINAL TRUSS INTERBODY FUSION DEVICE
| Applicant | 4-Web Spine, LLC, Apple Valley MN, US |
| Decision | Substantially Equivalent, Jan 18, 2011 |
| Received | Dec 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083894
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.