FDA 510(k) Application Details - K020240

Device Classification Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component   More FDA Info for this Device
510(K) Number	K020240
Device Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Applicant	PLUS ORTHOPEDICS 6055 LUSK BLVD. SAN DIEGO, CA 92121-2700 US Other 510(k) Applications for this Company
Contact	HARTMUT LOCH 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	01/23/2002
Decision Date	02/22/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review