K-number	K162189
Device name	ANAX 5.5 Spinal System
Applicant	U&I Corporation
Product code	MNH
Device class	Class II
Decision date	Aug 30, 2016
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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ANAX 5.5 Spinal System

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ANAX 5.5 Spinal System