K-number	K151863
Device name	Precision Spine Interspinous Plate System
Applicant	Precision Spine, Inc.
Product code	PEK
Device class	Class II
Decision date	Aug 7, 2015
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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Precision Spine Interspinous Plate System

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