510(k) K202872 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Prase PEEK Anterior Cervical Interbody Spacer
| Applicant | Gbs Commonwealth Co., Ltd., Geumcheon-Gu, KR |
| Decision | Substantially Equivalent, Feb 4, 2021 |
| Received | Sep 28, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202872
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.