FDA 510(k) Application Details - K013132

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K013132
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	SURGICAL IMPLANT GENERATION NETWORK (SIGN) 2950 GEORGE WASHINGTON WAY RICHLAND, WA 99352-1615 US Other 510(k) Applications for this Company
Contact	DOUG DONNELLY 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	09/19/2001
Decision Date	12/20/2001
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