K-number	K151140
Device name	LnK Lumbar Interbody Fusion Cage System
Applicant	L&K BIOMED Co., Ltd.
Product code	MAX
Device class	Class II
Decision date	Aug 18, 2015
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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LnK Lumbar Interbody Fusion Cage System

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