510(k) K121567 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM
| Applicant | Accel Spine, Dallas TX, US |
| Decision | Substantially Equivalent, Sep 26, 2012 |
| Received | May 29, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121567
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.