Note by the author: 75% of 104 Scientific References related to TWA are not older than 10 years, and 81% of them are not older than 5 years.
Case presentationThis is to inform the community of all Orthopaedic and Hand Surgeons around the world who are interested in Total Wrist Arthroplasty (TWA) about the official decision by the European and German Branches (Winterthur, Switzerland and Freiburg i. Breisgau, Germany) of the company for distribution (Zimmer Biomet Holdings Inc., Warsaw, Indiana/USA) for the Maestro TM Wrist Reconstructive System (WRS, insertion of the carpal plate with variable or fixed locking screws) (Figure 1A-C). Recently, the company informed the author on February 26., 2018 that they have definitively withdrawn the Maestro TM WRS from the marketplace here in Germany, and this decision will be extended in 2018 for all other countries worldwide if the CE certification is finished in these countries in 2018 as well. The company officially wrote that the cause for its withdrawal is that as follows: The Maestro TM WRS is approved only for its cemented use by the US Food and Drug Administration (FDA) and there are no publications in the literature worldwide on favorable results with its cemented use, and so, it cannot be guaranteed the surveillance of this implant by the company if it inserted in a non-cemented manner (i.e. "off-label" use).