K-number	K972053
Device name	PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM
Applicant	Lunar Corp.
Product code	KGI
Device class	Class II
Decision date	Aug 8, 1997
Decision	Substantially Equivalent
Regulation	892.1170

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View the full FDA submission: accessdata.fda.gov

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PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM

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