FDA 510(k) Application Details - K991806

Device Classification Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component   More FDA Info for this Device
510(K) Number	K991806
Device Name	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Applicant	WALTER ABENDSCHEIN, M.D. 5530 WISCONSIN AVE. SUITE 705 CHEVY CHASE, MD 20815 US Other 510(k) Applications for this Company
Contact	WALTER ABENDSCHEIN 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	05/26/1999
Decision Date	08/06/1999
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