510(k) K131296 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VARILIFT-L INTERBODY FUSION DEVICE
| Applicant | Wenzel Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Sep 3, 2013 |
| Received | May 6, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131296
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.