FDA 510(k) Application Details - K960653

Device Classification Name	Suture, Absorbable, Synthetic   More FDA Info for this Device
510(K) Number	K960653
Device Name	Suture, Absorbable, Synthetic
Applicant	ETHICON, INC. ROUTE 22 WEST P.O. BOX 151 SOMERVILLE, NJ 08876-0151 US Other 510(k) Applications for this Company
Contact	JOHN D PAULSON, PH.D. Other 510(k) Applications for this Contact
Regulation Number	878.4830   More FDA Info for this Regulation Number
Classification Product Code	GAN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/15/1996
Decision Date	03/28/1996
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