K-number	K201314
Device name	Restor3d Utility Wedge
Applicant	Restor3D, Inc.
Product code	PLF
Device class	Class II
Decision date	Jun 17, 2021
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Restor3d Utility Wedge

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