K-number	K181410
Device name	MotoCLIP/HiMAX Implant System
Applicant	Crossroads Extremity Systems, LLC
Product code	JDR
Device class	Class II
Decision date	Jun 29, 2018
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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MotoCLIP/HiMAX Implant System

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