FDA 510(k) Application Details - K230783

Device Classification Name	Orthopedic Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K230783
Device Name	Orthopedic Stereotaxic Instrument
Applicant	Remex Medical Corp. 4F., No. 9, Jingke Road, Nantun Dist. Taichung City 408209 TW Other 510(k) Applications for this Company
Contact	Wang Cheng-Hsiung Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	OLO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2023
Decision Date	04/21/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review