510(k) K133721 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INFILL 41-TLIF CONVEX OBLIQUE DEVICE, INFILL 43-TLIF CONTOUR OBLIQUE, INFILL 44-TLIF CONTOUR OBLIQUE AND THE INFILL 60
| Applicant | Pinnacle Spine Group, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Mar 31, 2014 |
| Received | Dec 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133721
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.