510(k) K222004 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
INTEGRATE -C Interbody Fusion System
| Applicant | Happe Spine, Grand Rapids MI, US |
| Decision | Substantially Equivalent, Apr 28, 2023 |
| Received | Jul 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222004
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.