510(k) K171075 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Calix-C Cervical Interbody Spacer
| Applicant | X-Spine Systems, Inc., Miamisburg OH, US |
| Decision | Substantially Equivalent, Aug 1, 2017 |
| Received | Apr 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171075
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.