510(k) K122037 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ANATOMIC PEEK CERVICAL FUSION SYSTEM CORNERSTONE PSR CERVICAL FUSION SYSTEM PEEK PREVAIL CERVICAL INTERBODY DEVICE CAPST
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Mar 22, 2013 |
| Received | Jul 11, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122037
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.