K-number	K162220
Device name	DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage
Applicant	Dio Medical Co., Ltd.
Product code	ODP
Device class	Class II
Decision date	Nov 21, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage

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