510(k) K131880 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM
| Applicant | Spinefrontier, Inc., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Jan 3, 2014 |
| Received | Jun 25, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K131880
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.