K-number	K223804
Device name	PercuNav Image Fusion and Interventional Navigation System
Applicant	Philips Ultrasound, LLC
Product code	JAK
Device class	Class II
Decision date	Jan 18, 2023
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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PercuNav Image Fusion and Interventional Navigation System

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