K-number	K220142
Device name	BRM Digitalis Spacer
Applicant	Brm Extremities Srl
Product code	KYJ
Device class	Class II
Decision date	Apr 4, 2023
Decision	Substantially Equivalent
Regulation	888.3230

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Source

View the full FDA submission: accessdata.fda.gov

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BRM Digitalis Spacer

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