FDA 510(k) Application Details - K013334

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K013334
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	ARTHOCARE CORPORATION 38 FREEMANS WAY HARROGATE, NORTH YORKSHIRE HG3 2QF GB Other 510(k) Applications for this Company
Contact	NICK WOODS 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	10/09/2001
Decision Date	12/13/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review