FDA 510(k) Application Details - K211939

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K211939
Device Name	Accelerator, Linear, Medical
Applicant	Brainlab AG Olof-Palme-Str. 9 Munich 81829 DE Other 510(k) Applications for this Company
Contact	Chiara Cunico Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	IYE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/23/2021
Decision Date	07/22/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review