510(k) K162220 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage
| Applicant | Dio Medical Co., Ltd., Sagimakgol-Ro Jungwon-Gu Seongnam-Si, KR |
| Decision | Substantially Equivalent, Nov 21, 2016 |
| Received | Aug 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162220
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.