MRI Safety information for:
NUVASIVE COHERE THORACOLUMBAR INTERBODY SYSTEM
NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
Polymeric spinal interbody fusion cage
In accordance with ASTM F2503 Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment, NuVasive, Inc.'s Cohere Thoracolumbar Interbody System product line should be labeled MR Conditional, following analysis comparing Cohere Thoracolumbar interbody devices to non-clinically tested MR Conditional devices. Non-clinical analysis has demonstrated that the Cohere devices are MR Conditional. A patient with this device can be safely scanned in an MR system with the following conditions: