K-number	K201259
Device name	ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System
Applicant	Wrightmedicaltechnologyinc
Product code	HRS
Device class	Class II
Decision date	Jan 8, 2021
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System

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