K-number	K133066
Device name	SPINESELECT POLYSCREW PEDICLE SCREW SYSTEM
Applicant	Spineselect, LLC
Product code	NKB
Device class	Class II
Decision date	Jan 13, 2014
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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SPINESELECT POLYSCREW PEDICLE SCREW SYSTEM

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