K-number	K242364
Device name	IdentiTi II Interbody System
Applicant	Alphatec Spine, Inc.
Product code	MAX
Device class	Class II
Decision date	Oct 4, 2024
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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IdentiTi II Interbody System

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IdentiTi II Interbody System