K-number	K200953
Device name	NuVasive® Cohere® Thoracolumbar Interbody System
Applicant	Nu Vasive, Incorporated
Product code	MAX
Device class	Class II
Decision date	Oct 6, 2020
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive® Cohere® Thoracolumbar Interbody System

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