Fournitures Hospitalieres Industrie

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K171789ARROW Reverse Porous GlenoidJanuary 23, 2018
K163148BePOD® Foot ScrewsSeptember 14, 2017
K163710BePOD® EZ Weil ScrewsSeptember 8, 2017
K162068ARROW Anatomical Porous glenoidApril 10, 2017
K170040BePOD Cannulated Arthrodesis ScrewsApril 4, 2017
K150568ARROW Humeral stems size 6 and 16October 29, 2015
K150471CalcaNail Orthopedic Arthrodesis NailMay 22, 2015
K150463CalcaNail Orthopedic NailMay 22, 2015
K142778ARROW Reverse Shoulder long keel and short keel glenoid baseMarch 20, 2015
K120740COLS® FIXATION SYSTEMMarch 5, 2013
K112193ARROW REVERSE SHOULDER SYSTEMJuly 12, 2012
K113591COLS PEEKDecember 22, 2011
K093599ARROW ANATOMICAL SHOULDER SYSTEMNovember 24, 2010
K080974TLS FIXATION SYSTEMJuly 1, 2008
K070617CANNULATED SCREWJune 14, 2007
K060367TENOLIGAugust 9, 2006
K052058MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAILAugust 22, 2005
K050556ALUMINA HEADMay 11, 2005
K042035ALUMINA HEADNovember 17, 2004
K042332TITANIUM TELEGRAPH HUMERAL NAILOctober 7, 2004