K-number	K112757
Device name	PIONEER POSTERIOR CERVICO THORACIC SYSTEM
Applicant	Pioneer Surgical Technology, Inc.
Product code	KWP
Device class	Class II
Decision date	Mar 12, 2012
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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PIONEER POSTERIOR CERVICO THORACIC SYSTEM

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