FDA 510(k) Application Details - K113380

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K113380
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	MEDTRONIC INC. 7000 CENTRAL AVENUE NE MINNEAPOLIS, MN 55432-3576 US Other 510(k) Applications for this Company
Contact	THOMAS REICHEL 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	11/16/2011
Decision Date	11/15/2012
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