CD HORIZON Spinal SystemRecalls & reported problems across all models
Medtronic Sofamor Danek, Inc. · 342 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
CD HORIZON Spinal System models — page 4
342 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- CD HORIZON® Spinal System 54840045540APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 54840045535APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System X1013202INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- CD HORIZON® Spinal System X0212548APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 6640007APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- 1 report
- CD HORIZON® Spinal System 5135251ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- CD HORIZON® Spinal System 859-550Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 96509HTOrthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 8672065Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- CD HORIZON® Spinal System 8115516APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 8115525Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 8115530APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 8116425APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 8116436Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 8116458Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 7543650APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 7543745Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System RBT043301Orthopedic stereotaxic instrument1 report
- CD HORIZON® Spinal System RBT011006Orthopedic stereotaxic instrument1 report
- CD HORIZON® Spinal System 559200003Appliance, fixation, spinal intervertebral body1 report
- CD HORIZON® Spinal System RBT076210Orthopedic stereotaxic instrument1 report
- CD HORIZON® Spinal System G5932105656APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 7575550APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 7041430APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 7576535APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 7576555Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 7577555APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 869-021ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- CD HORIZON® Spinal System 75447535Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 75447545Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 75447550APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 75447570ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- CD HORIZON® Spinal System 75495540Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 75495545ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- CD HORIZON® Spinal System 76446535APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 76446540APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 75496550APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- CD HORIZON® Spinal System 7560020Orthosis, spondylolisthesis spinal fixation1 report
- CD HORIZON® Spinal System 7191540APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD HORIZON® Spinal System 99460040APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CD Horizon® Spinal System 7078398Appliance, fixation, spinal intervertebral body1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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