510(k) K100820 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM
| Applicant | Wenzel Spine, Austin TX, US |
| Decision | Substantially Equivalent, Aug 5, 2010 |
| Received | Mar 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100820
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.