K-number	K203832
Device name	FuseForce Flex Dynamic Compression System
Applicant	Wright Medical
Product code	JDR
Device class	Class II
Decision date	May 7, 2021
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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FuseForce Flex Dynamic Compression System

Everything you need for a 510(k) submission. Nothing you don't.

FuseForce Flex Dynamic Compression System