510(k) K122989 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BIOMET LATERAL SPACER SYSTEM
| Applicant | Biomet Spine (Aka Ebi, LLC), Parsippany NJ, US |
| Decision | Substantially Equivalent, Oct 24, 2012 |
| Received | Sep 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122989
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.