A Multi-Center Post-Market Data Collection Protocol to Evaluate the Performance of Orthofix Spine Devices

Authors
Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2021
This protocol is designed to study Orthofix regulatory approved and commercially available spine devices to generate Real World Evidence (RWE) of device safety and performance in the treatment of patients with spine injuries and/or disorders following the local medical standard of care. The clinical data generated from this study will support compliance to global regulatory requirements including but not limited to the European Medical Device Regulation (EU MDR) for the applicable devices.
Epistemonikos ID: b304f93ad22bbb8883087ba4839a4dfb06995b34
First added on: May 09, 2024