FDA 510(k) Application Details - K202404

Device Classification Name	More FDA Info for this Device
510(K) Number	K202404
Device Name	BoneMRI
Applicant	MRIguidance B.V Gildstraat 91a Utrecht 3572 EL NL Other 510(k) Applications for this Company
Contact	Roel Raatgever Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/21/2020
Decision Date	12/22/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review