510(k) K100743 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ATLAS SPINE PIVOTING SYSTEM
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Aug 10, 2010 |
| Received | Mar 16, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100743
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.