Avis De Sécurité sur procarve; 3r2 procarve knee joint, 1e2 procarve foot standard, 1e2 = 1 procarve foot firmdevices for knee and foot prosthesis.

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.