510(k) K223043 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
The Integrity Spine Core System
| Applicant | Integrity Spine, San Antonio TX, US |
| Decision | Substantially Equivalent, Mar 20, 2023 |
| Received | Sep 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223043
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.