K-number	K132049
Device name	THUNDERBOLT AND LANCER PEDICLE SCREW SYSTEMS
Applicant	Choicespine
Product code	NKB
Device class	Class II
Decision date	Aug 15, 2014
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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THUNDERBOLT AND LANCER PEDICLE SCREW SYSTEMS

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