510(k) K202302 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Atlas Spine Rebar (Ti) Spacer System
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Oct 30, 2020 |
| Received | Aug 14, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202302
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.