510(k) K123281 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ACCULIF TL-PEEK CAGE
| Applicant | Coalign Innovations, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jan 23, 2013 |
| Received | Oct 22, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123281
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.