K-number	K202812
Device name	IdentiTi Cervical Standalone Interbody System
Applicant	Alphatec Spine, Inc.
Product code	OVE
Device class	Class II
Decision date	Dec 18, 2020
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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IdentiTi Cervical Standalone Interbody System

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