K-number	K051275
Device name	LAGUNA MONOAXIAL PEDICLE SCREW SYSTEM
Applicant	Allez Spine, LLC
Product code	NKB
Device class	Class II
Decision date	Dec 9, 2005
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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LAGUNA MONOAXIAL PEDICLE SCREW SYSTEM

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