FDA 510(k) Application Details - K130907

Device Classification Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component   More FDA Info for this Device
510(K) Number	K130907
Device Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Applicant	Stryker Trauma AG 325 Corporate Drive Mahwah, NJ 07430 US Other 510(k) Applications for this Company
Contact	ESTELA CELI Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	KTT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/01/2013
Decision Date	06/10/2013
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