The NeuroCybernetic Prosthesis System is a vagus nerve stimulator, consisting of a generator which is implanted under the collar bone like a pacemaker and connected by wire to the vagus nerve in the neck where it delivers electrical signals to the brain to control seizures. It includes an external programming system which is used by the physician to change stimulation settings. Patients can turn the stimulator on and off with a hand-held magnet by holding it over the stimulator.

Approved by the U.S. Food and Drug Administration (FDA) in 1997, the NeuroCybernetic Prosthesis System, made by Cyberonics, of Houston, is intended for use in conjunction with drugs or surgery in adults and adolescents with partial onset seizures, the type of seizures that begin in one part of the brain and may remain localized or become generalized to the entire brain.

In March 2001, the FDA sent a warning letter to Cyberonics after receiving reports of 83 deaths and dozens of infections linked to the NeuroCybernetic Prosthesis System. In the letter, the FDA accused the company of improperly reporting and recording the adverse events and of failing to investigate the cause of the deaths.

If you have suffered injuries due to the NeuroCybernetic Prosthesis System, it may be important to contact an attorney who can help you protect your legal rights. Please keep in mind that there may be time limits within which you must commence suit.

Attorneys associated with InjuryBoard.com will evaluate your case free of charge. In addition, you will not pay any fees unless your attorney recovers money for you. Please click on the free Ask An Attorney button to take advantage of this valuable service.

Information Provided by the U.S. Food and Drug Administration

See Also

  1. Medical Devices & Implants
  2. Infections
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