510(k) K142026 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Spinefrontier, Inc., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Oct 20, 2014 |
| Received | Jul 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142026
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.