510(k) K122639 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SYNTHES SYNCAGE EVOLUTION SPACER
| Applicant | Synthes (USA) Products, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, May 24, 2013 |
| Received | Aug 29, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122639
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.