K-number	K171690
Device name	Trident Extremity Fixation System
Applicant	Trident Orthopedics
Product code	HRS
Device class	Class II
Decision date	May 8, 2018
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Trident Extremity Fixation System

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