The following data is part of a premarket notification filed by Dio Medical Co., Ltd with the FDA for Dio Medical Iva (acif, Dlif, Plif, Tlif,and Alif) Cage.
| Device ID | K162220 |
| 510k Number | K162220 |
| Device Name: | DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | DIO MEDICAL CO., LTD 101-105 MEGACENTER, SK TECHNOPARK, Sagimakgol-ro Jungwon-gu Seongnam-si, KR 124 |
| Contact | Sung Hee-lee |
| Correspondent | Paul Speidel RQMIS INC 110 HAVERHILL RD, SUITE 526 Amesbury, MA 01913 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-08-08 |
| Decision Date | 2016-11-21 |
| Summary: | summary |