FDA 510(k) Application Details - K960481

Device Classification Name	Mesh, Surgical, Polymeric   More FDA Info for this Device
510(K) Number	K960481
Device Name	Mesh, Surgical, Polymeric
Applicant	TISSUE TECHNOLOGIES, INC. 1370 GREEN ST. SAN FRANCISO, CA 94109 US Other 510(k) Applications for this Company
Contact	JESSE KRAMER Other 510(k) Applications for this Contact
Regulation Number	878.3300   More FDA Info for this Regulation Number
Classification Product Code	FTL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/02/1996
Decision Date	04/01/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review