FDA 510(k) Application Details - K970292

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K970292
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	INFLUENCE, INC. 601 MONTGOMERY ST., SUITE 845 SAN FRANCISCO, CA 94111 US Other 510(k) Applications for this Company
Contact	PETER BICK Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	MBI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/24/1997
Decision Date	04/23/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review