K-number	K162693
Device name	VertebraLINK Fusion Platform
Applicant	Facetlink Dba Linkspine
Product code	MAX
Device class	Class II
Decision date	Mar 29, 2017
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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VertebraLINK Fusion Platform

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