FDA 510(k) Application Details - K201435

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K201435
Device Name	Neurological Stereotaxic Instrument
Applicant	Therataxis, LLC Johns Hopkins Eastern Building Suite B305 1101 East 33rd Street Baltimore, MD 21218 US Other 510(k) Applications for this Company
Contact	Raghu Raghavan Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	HAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/01/2020
Decision Date	12/03/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review