FDA 510(k) Application Details - K151405

Device Classification Name	Scalpel, Ultrasonic, Reprocessed   More FDA Info for this Device
510(K) Number	K151405
Device Name	Scalpel, Ultrasonic, Reprocessed
Applicant	Surgical Instrument Services and Savings(dba Medline ReNewal 2747 SW 6th St. Redmond, OR 97756 US Other 510(k) Applications for this Company
Contact	Brandi Panteleon Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	NLQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/26/2015
Decision Date	01/26/2016
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