User's Manual

Safety Information
Precision Spectra™ System Information for Patients
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• Undesirable stimulation may occur over time due to cellular changes in tissue around the
electrodes, changes in electrode position, loose electrical connections and/or lead failure.
• You may experience painful electrical stimulation of your chest wall as a result of
stimulation of certain nerve roots several weeks after surgery.
• Over time, your implant may move from its original position.
• You may experience weakness, clumsiness, numbness or pain below the level of
implantation.
• You may experience persistent pain at the Stimulator or lead site.
In any event, you should contact your physician and inform him/her.
FCC Rules
The following is federal government communications regulation information about the Precision
Spectra™ Spinal Cord Stimulation System.
This device complies with part 15 of the FCC Rules. Operation is subject to the following two
conditions: (1) This device may not cause harmful interference, and (2) This device must accept any
interference received including interference that may cause undesired operation.