510(k) K163494 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Summit Spine Channel Cervical Interbody Fusion System
| Applicant | Summit Spine, Georgetown TX, US |
| Decision | Substantially Equivalent, Jun 20, 2017 |
| Received | Dec 13, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163494
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.