510(k) K103666 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LANX LATERAL
| Applicant | Lanx, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Mar 23, 2011 |
| Received | Dec 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103666
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.