510(k) K120275 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SYNTHES ACIS/VERTEBRAL SPACER CR
| Applicant | Synthes (Usa), LLC, West Chester PA, US |
| Decision | Substantially Equivalent, May 25, 2012 |
| Received | Jan 30, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120275
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.