Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Fournitures Hospitalieres Industrie

FDA 510(k) & PMA Approved Devices — 20 products

Total Devices20
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K171789 ARROW Reverse Porous GlenoidPHX2018-01-23 View
510(k) K163148 BePOD® Foot ScrewsHWC2017-09-14 View
510(k) K163710 BePOD® EZ Weil ScrewsHWC2017-09-08 View
510(k) K162068 ARROW Anatomical Porous glenoidMBF2017-04-10 View
510(k) K170040 BePOD Cannulated Arthrodesis ScrewsHWC2017-04-04 View
510(k) K120740 COLS® FIXATION SYSTEMMBI2013-03-05 View
510(k) K112193 ARROW REVERSE SHOULDER SYSTEMPHX2012-07-12 View
510(k) K113591 COLS PEEKHWC2011-12-22 View
510(k) K093599 ARROW ANATOMICAL SHOULDER SYSTEMKWS2010-11-24 View
510(k) K080974 TLS FIXATION SYSTEMHWC2008-07-01 View
510(k) K070617 CANNULATED SCREWHWC2007-06-14 View
510(k) K060367 TENOLIGGAT2006-08-09 View
510(k) K052058 MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAILHSB2005-08-22 View
510(k) K050556 ALUMINA HEADLZO2005-05-11 View
510(k) K042035 ALUMINA HEADLZO2004-11-17 View
510(k) K042332 TITANIUM TELEGRAPH HUMERAL NAILHSB2004-10-07 View
510(k) K041456 SNAP-OFF SCREWSHWC2004-08-25 View
510(k) K031939 BIO-EUROLIG INTERFERENCE SCREWHWC2004-06-24 View
510(k) K033510 MODIFICATION TO TELEGRAPH HUMERAL NAILHSB2003-12-03 View
510(k) K023241 TELEGRAPH HUMERAL NAILHSB2002-12-24 View
↑