K-number	K102020
Device name	VEGA SPAN SPINOUS PROCESS PLATE SYSTEM
Applicant	Spinefrontier, Inc.
Product code	KWP
Device class	Class II
Decision date	Sep 1, 2010
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

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