FDA 510(k) Application Details - K233866

Device Classification Name	System,Surgical,Computer Controlled Instrument   More FDA Info for this Device
510(K) Number	K233866
Device Name	System,Surgical,Computer Controlled Instrument
Applicant	Asensus Surgical, Inc. 1 TW Alexander Dr Suite 160 Durham, NC 27703 US Other 510(k) Applications for this Company
Contact	Madhuvanthi Soundirarajan Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	NAY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/06/2023
Decision Date	07/19/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review