FDA 510(k) Application Details - K171789

Device Classification Name	More FDA Info for this Device
510(K) Number	K171789
Device Name	ARROW Reverse Porous Glenoid
Applicant	Fournitures Hospitalieres Industrie ZI de Kernevez - 6 rue Nobel Quimper 29000 FR Other 510(k) Applications for this Company
Contact	Patricia Donnard Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PHX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/15/2017
Decision Date	01/23/2018
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