510(k) K121178 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
TRANSCORP ACIF SYSTEM
| Applicant | Transcorp, Inc., Byron Center MI, US |
| Decision | Substantially Equivalent, Jul 5, 2013 |
| Received | Apr 18, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121178
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.