K-number	K143278
Device name	LnK Posterior Cervical Fixation System
Applicant	L&K BIOMED Co., Ltd.
Product code	KWP
Device class	Class II
Decision date	Jul 29, 2015
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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LnK Posterior Cervical Fixation System

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