510(k) K191812 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ADI Cervical Interbody Fusion Device
| Applicant | Additive Device, Inc. (Adi) D/B/A Restor3D, Durham NC, US |
| Decision | Substantially Equivalent, Oct 24, 2019 |
| Received | Jul 5, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191812
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.