510(k) K082774 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Lanx, LLC, Broomfield CO, US |
| Decision | Substantially Equivalent, Oct 21, 2008 |
| Received | Sep 22, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082774
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.