Canadian data is current through March 2018. All of the data comes from Health Canada, 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 recall data from the U.S. and Canada.
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A labelling correction was being initiated that affected the above reference part number and document number due to a review of the technique guide showing an identified need for additional clarification in the application notes for the tomofix medial high tibia plate technique guide.