FDA 510(k) Application Details - K223488

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K223488
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	Medtronic, Inc. 2300 Berkshire Lane North Plymouth, MN 55441 US Other 510(k) Applications for this Company
Contact	Aditi Dave Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/21/2022
Decision Date	03/23/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review