FDA 510(k) Application Details - K101997

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K101997
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	ELLIPSE TECHNOLOGIES, INC. 13844 ALTON PARKWAY SUITE 130 IRVINE, CA 92618 US Other 510(k) Applications for this Company
Contact	John McIntyre 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	07/15/2010
Decision Date	07/12/2011
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