FDA 510(k) Application Details - K082833

Device Classification Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component   More FDA Info for this Device
510(K) Number	K082833
Device Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Applicant	NUTEK ORTHOPAEDICS, INC. 16771 SW 6TH ST. PEMBROKE PINES, FL 33027 US Other 510(k) Applications for this Company
Contact	PETER MINCIELLI 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	09/26/2008
Decision Date	02/05/2009
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