510(k) K162212 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DIVERGENCE-L ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, May 19, 2017 |
| Received | Aug 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162212
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.