510(k) K133623 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
C-PLUS
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Feb 10, 2014 |
| Received | Nov 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133623
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.