K-number	K030197
Device name	BLACKSTONE POSTERIOR CERVICAL SYSTEM
Applicant	Blackstone Medical, Inc.
Product code	KWP
Device class	Class II
Decision date	Jun 12, 2003
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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BLACKSTONE POSTERIOR CERVICAL SYSTEM

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