K-number	K131878
Device name	LLIAD, KORA, ZENIUS PEDICLE SCREW SYSTEM
Applicant	Medyssey USA, Inc.
Product code	NKB
Device class	Class II
Decision date	Aug 23, 2013
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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LLIAD, KORA, ZENIUS PEDICLE SCREW SYSTEM

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