FDA 510(k) Application Details - K082729

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K082729
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	ANULEX TECHNOLOGIES, INC 5600 ROWLAND ROAD, STE 280 MINNETONKA, MN 55343 US Other 510(k) Applications for this Company
Contact	RACHEL KENNEDY 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	09/18/2008
Decision Date	12/19/2008
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