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 categorySpinal vertebral body replacement device - Cervical
Device ID00887517267207
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information