FDA 510(k) Application Details - K223770

Device Classification Name	Instrument, Ultrasonic Surgical   More FDA Info for this Device
510(K) Number	K223770
Device Name	Instrument, Ultrasonic Surgical
Applicant	Stryker Corporation 1941 Stryker Way Kalamazoo, MI 49002 US Other 510(k) Applications for this Company
Contact	Thomas Flannelly Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LFL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/15/2022
Decision Date	02/16/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review