510(k) K233084 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Peridot-PT Anterior Cervical Intervertebral body fusion System, Peridot-PT Intervertebral body fusion system
| Applicant | Gbs Commonwealth Co., Ltd., Geumcheon-Gu, KR |
| Decision | Substantially Equivalent, Nov 21, 2023 |
| Received | Sep 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233084
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.