FDA 510(k) Application Details - K160693

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K160693
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	STRYKER CORPORATION 4100 E. MILHAM AVENUE KALAMAZOO, MI 49001 US Other 510(k) Applications for this Company
Contact	MAIREAD TWOMEY 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	03/14/2016
Decision Date	04/13/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review