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 |