510(k) K143297 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical Interbody Fusion System, InFix Anterior Lumbar System, TraXis Vertebral Body Replacement (Ti and VUE)
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 12, 2015 |
| Received | Nov 17, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143297
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.