K-number	K200981
Device name	Mega Plus MIS Spine System
Applicant	Bk Meditech, Co., Ltd.
Product code	NKB
Device class	Class II
Decision date	Aug 11, 2020
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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Mega Plus MIS Spine System

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