Field Safety Notices about nails for panta arthrodesis from 500 050 to 500 380; nails for panta xl arthrodesis from 510 111 to 510 341 fixation devices, orthopedic surgery

Italian data is current through August 2018. All of the data comes from Ministero della Salute (Health Ministry), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Italy.