510(k) K081636 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PEEK-OPTIMA ALIF SPACER
| Applicant | Biomet Spine, Parsippany NJ, US |
| Decision | Substantially Equivalent, Aug 7, 2008 |
| Received | Jun 11, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081636
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.