K-number	K111290
Device name	PIEZO BONE SURGERY
Applicant	Guilin Woodpecker Medical Instrument Co., Ltd.
Product code	DZI
Device class	Class II
Decision date	Nov 18, 2011
Decision	Substantially Equivalent
Regulation	872.4120

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Source

View the full FDA submission: accessdata.fda.gov

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PIEZO BONE SURGERY

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