510(k) K121649 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CONSTRUX MINI PEEK TI SPACER SYSTEM
| Applicant | Orthofix, Lewisville TX, US |
| Decision | Substantially Equivalent, Nov 29, 2012 |
| Received | Jun 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121649
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.