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.
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Primary Safety Assessment: Device or procedure related adverse events
Timeframe: Pre-Operative to up to 10-years Post-Operative
Primary Effectiveness Assessments: Fusion status measured radiographs
Timeframe: Intra-operative to up to 10-years Post-Operative
Primary Effectiveness Assessment
Timeframe: Intra-operative to up to 10-years Post-Operative
Primary Effectiveness Assessment
Timeframe: Intra-operative to up to 10-years Post-Operative