K-number	K181257
Device name	PlasmaBlade X 3.0S, PlasmaBlade X 4.0
Applicant	Medtronic Advanced Energy
Product code	GEI
Device class	Class II
Decision date	Aug 2, 2018
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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PlasmaBlade X 3.0S, PlasmaBlade X 4.0

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