K-number	K200817
Device name	URIS OMNI Narrow System & Prosthetic
Applicant	Truabutment, Inc.
Product code	DZE
Device class	Class II
Decision date	Oct 7, 2020
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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URIS OMNI Narrow System & Prosthetic

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