K-number	K160723
Device name	OnSight 3D Extremity System
Applicant	Carestream Health, Inc.
Product code	JAK
Device class	Class II
Decision date	Aug 30, 2016
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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OnSight 3D Extremity System

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