K-number	K230478
Device name	Acro Composites Interbody System
Applicant	Acro Composites, LLC
Product code	ODP
Device class	Class II
Decision date	Oct 19, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Acro Composites Interbody System

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