K-number	K121136
Device name	RENOIR POSTERIOR CERVIAL FIXATION SYSTEM
Applicant	Accel Spine
Product code	KWP
Device class	Class II
Decision date	Aug 9, 2012
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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RENOIR POSTERIOR CERVIAL FIXATION SYSTEM

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