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 |