K-number	K213813
Device name	DuraFuse Clip and Applier System
Applicant	Neuramedica, Inc.
Product code	FZP
Device class	Class II
Decision date	Jul 22, 2022
Decision	Substantially Equivalent
Regulation	878.4300

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Source

View the full FDA submission: accessdata.fda.gov

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DuraFuse Clip and Applier System

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