FDA 510(k) Application Details - K250728

Device Classification Name	Laparoscope, General & Plastic Surgery   More FDA Info for this Device
510(K) Number	K250728
Device Name	Laparoscope, General & Plastic Surgery
Applicant	Arthrex, Inc. 1370 Creekside Boulevard Naples, FL 34108 US Other 510(k) Applications for this Company
Contact	Lai Saeteurn Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	GCJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/11/2025
Decision Date	05/05/2025
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