510(k) K131242 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ARDIS INTERBODY SYSTEM
| Applicant | Zimmer Spine, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 3, 2013 |
| Received | May 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131242
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.