K-number	K163428
Device name	HA Minuteman G3-R MIS Fusion Plate
Applicant	Spinal Simplicity
Product code	PEK
Device class	Class II
Decision date	Feb 2, 2017
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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HA Minuteman G3-R MIS Fusion Plate

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