K-number	K132740
Device name	SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM
Applicant	Spinefrontier, Inc.
Product code	NQW
Device class	Class II
Decision date	Nov 26, 2013
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM

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