K-number	K211173
Device name	maxmorespine Bipolar Electrodes
Applicant	Hoogland Spine Products, GmbH
Product code	GEI
Device class	Class II
Decision date	Jun 23, 2022
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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maxmorespine Bipolar Electrodes

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