OssDsign receives approval to establish a clinical registry in the U.S. to collect real-world data on OssDsign Catalyst
Uppsala, January 13th, 2022. OssDsign AB (publ.) today announces that the Western Institutional Review Board (WIRB), one of the largest institutional research review organizations in the U.S., has approved the company’s application to establish PROPEL, a multi-centre, prospective spinal fusion registry, providing opportunity to study real-world data from patients who have been treated with OssDsign Catalyst.OssDsign Catalyst received FDA clearance in 2020 and was launched in the U.S. in August 2021. During 2022, clinics will gradually be enrolled to the registry, with the objective to