MRI Safety information for:

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’s CoRoent Thoracolumbar devices are labeled MR Conditional. NuVasive, Inc.’s CoRoent Thoracolumbar is manufactured of non-ferromagnetic Titanium. Non-clinical testing has demonstrated that the CoRoent Thoracolumbar device is MR-Conditional. Patients can be scanned safely immediately after implantation under the following conditions: