FDA 510(k) Application Details - K120943

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K120943
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	ARTHROCARE CORPORATION 7000 WEST WILLIAM CANNON DRIVE BUILDING ONE AUSTIN, TX 78735-0000 US Other 510(k) Applications for this Company
Contact	CHERYL FREDRICK 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	03/29/2012
Decision Date	09/21/2012
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