510(k) K130194 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ACCULIF XL CAGE
| Applicant | Coalign Innovations, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Apr 3, 2013 |
| Received | Jan 28, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130194
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.