FDA 510(k) Application Details - K173043

Device Classification Name	Suture, Absorbable, Synthetic, Polyglycolic Acid   More FDA Info for this Device
510(K) Number	K173043
Device Name	Suture, Absorbable, Synthetic, Polyglycolic Acid
Applicant	Nantong Holycon Medical Devices Co., Ltd. No.66, Zhongyang Road, Economic Technology Department Area Nantong 226009 CN Other 510(k) Applications for this Company
Contact	Feng Lu Other 510(k) Applications for this Contact
Regulation Number	878.4493   More FDA Info for this Regulation Number
Classification Product Code	GAM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2017
Decision Date	12/14/2017
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