K-number	K150856
Device name	Reform Pedicle Screw System
Applicant	Precision Spine, Inc.
Product code	NKB
Device class	Class II
Decision date	Jul 7, 2015
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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Reform Pedicle Screw System

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