K-number	K173030
Device name	Vertera Spine Cohere Cervical Interbody Fusion Device
Applicant	Nu Vasive, Incorporated
Product code	ODP
Device class	Class II
Decision date	Nov 21, 2017
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Vertera Spine Cohere Cervical Interbody Fusion Device

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