119. Adverse events associated the barricaid annular closure device: an analysis of the FDA MAUDE database

The Food and Drug Administration (FDA) maintains the Manufacturer and User Facility Device Experience (MAUDE) database for reporting adverse events associated with medical devices. This is a valuable tool for FDA-approved devices to follow the long-term complications associated with the device. Medical knowledge is currently limited of the adverse events associated with the annular closure device. This research aimed to evaluate adverse events related to this device, identify areas for improvement, reduce complications, and prevent future patient injury.
Source: The Spine Journal - Category: Orthopaedics Authors: Tags: Friday, October 20, 2023 7:30-9:00 Complications Source Type: research