K-number	K162134
Device name	ENNOVATE Spinal System
Applicant	Aesculap Implant Systems, LLC
Product code	NKB
Device class	Class II
Decision date	Dec 14, 2016
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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ENNOVATE Spinal System

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