K-number	K191047
Device name	ADI TiDAL Osteotomy Wedge
Applicant	Additive Device, Inc. (Adi) D/B/A Restor3D
Product code	PLF
Device class	Class II
Decision date	Nov 5, 2019
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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ADI TiDAL Osteotomy Wedge

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