510(k) K150135 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, Jun 11, 2015 |
| Received | Jan 21, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150135
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.