FDA 510(k) Application Details - K250505

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K250505
Device Name	Neurological Stereotaxic Instrument
Applicant	Phasor Health, LLC 8944 Kirby Drive Houston, TX 77054 US Other 510(k) Applications for this Company
Contact	Ray King 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	02/21/2025
Decision Date	07/09/2025
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