K-number	K103383
Device name	SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM
Applicant	Spartek Medical, Inc.
Product code	NKB
Device class	Class II
Decision date	Feb 17, 2011
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM

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