510(k) K142152 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CONSTRUX MINI PEEK; SPACER SYSTEM, TI SPACER SYSTEM, CERVICAL STAND ALONE SYSTEM
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, Jan 8, 2015 |
| Received | Aug 6, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142152
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.