FDA 510(k) Application Details - K023029

Device Classification Name	Suture, Nonabsorbable, Silk   More FDA Info for this Device
510(K) Number	K023029
Device Name	Suture, Nonabsorbable, Silk
Applicant	DEMETECH CORP. 12119 SW 131 AVE. MIAMI, FL 33186 US Other 510(k) Applications for this Company
Contact	LUIS ARGUELLO Other 510(k) Applications for this Contact
Regulation Number	878.5030   More FDA Info for this Regulation Number
Classification Product Code	GAP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/11/2002
Decision Date	11/25/2002
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