510(k) K222041 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
CYGNUS-C Standalone ACIF System
| Applicant | GS Medical Co., Ltd., Cheongju-Si, KR |
| Decision | Substantially Equivalent, Feb 9, 2023 |
| Received | Jul 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222041
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.