K-number	K203742
Device name	IdentiTi ALIF Standalone Interbody System
Applicant	Alphatec Spine, Inc.
Product code	OVD
Device class	Class II
Decision date	Apr 9, 2021
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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IdentiTi ALIF Standalone Interbody System

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