510(k) K231808 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
QUASAR Standalone ACIF System
| Applicant | GS Medical Co., Ltd., Cheongju-Si, KR |
| Decision | Substantially Equivalent, Jul 20, 2023 |
| Received | Jun 20, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231808
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.