FDA 510(k) Application Details - K020652

Device Classification Name	More FDA Info for this Device
510(K) Number	K020652
Device Name	HERNIAMESH T-SLING
Applicant	HERNIAMESH 8 ORANGE DR. JERICHO, NY 11753 US Other 510(k) Applications for this Company
Contact	LORENA TRABUCCO Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PAH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/28/2002
Decision Date	05/15/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review