K-number	K161303
Device name	dynaMX Compression Plate
Applicant	Mx Orthopedics, Corp.
Product code	HRS
Device class	Class II
Decision date	Jan 26, 2017
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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dynaMX Compression Plate

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dynaMX Compression Plate