FDA 510(k) Application Details - K173458

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K173458
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	Orthofix Srl Via Delle Nazioni 9 Bussolengo 37012 IT Other 510(k) Applications for this Company
Contact	Gianluca Ricadona 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	11/07/2017
Decision Date	12/07/2017
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