510(k) K122588 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VUSION CS PLUS
| Applicant | Ortho Development Corp., Draper UT, US |
| Decision | Substantially Equivalent, Jun 12, 2013 |
| Received | Aug 24, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122588
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.