Device typeSpinal implant trial: A copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device.
FDA categoryIntervertebral Fusion Device With Bone Graft, Cervical
Device IDM7391830707080
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information