K-number	K142217
Device name	Reliance Interspinous Plate System
Applicant	Reliance Medical Systems, LLC
Product code	PEK
Device class	Class II
Decision date	Apr 2, 2015
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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Reliance Interspinous Plate System

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