K-number	K171421
Device name	VERTICALE® Posterior Spinal Fixation System/VERTICALE® System
Applicant	Silony Medical GmbH
Product code	NKB
Device class	Class II
Decision date	Jan 10, 2018
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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VERTICALE® Posterior Spinal Fixation System/VERTICALE® System

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