FDA 510(k) Application Details - K962091

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K962091
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	ACUMED, INC. 10950 S.W. 5TH ST. SUITE 170 BEAVERTON, OR 97005 US Other 510(k) Applications for this Company
Contact	SHARI L JEFFERS Other 510(k) Applications for this Contact
Regulation Number	888.3020   More FDA Info for this Regulation Number
Classification Product Code	HSB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/29/1996
Decision Date	07/24/1996
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