510(k) K132852 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PEEK CAGE FOR THE VERTEBRAL SPINE
| Applicant | Neoortho Produtos Ortopedicos S/A, Aventura FL, US |
| Decision | Substantially Equivalent, May 29, 2014 |
| Received | Sep 11, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132852
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.