NM-787914-AA Indications to be used: The Boston Scientific Spinal Twine Stimulator Techniques are indicated as an assist while in the administration of Continual intractable pain in the trunk and/or limbs together with unilateral or bilateral pain associated with the next: failed back surgery syndrome, Complex Regional Pain Syndrome (CRPS) Styles I and II, intractable small back pain and leg pain, Diabetic Peripheral Neuropathy of your reduce extremities, radicular pain syndrome, radiculopathies causing pain secondary to failed back syndrome or herniated disc, epidural fibrosis, degenerative disc disorder (herniated disc pain refractory to conservative and surgical interventions), arachnoiditis, numerous back surgeries.

Warnings. Patients implanted with Boston Scientific Spinal Twine Stimulator Units with out ImageReady™ MRI Know-how should not be subjected to Magnetic Resonance Imaging (MRI). Publicity to MRI may cause dislodgement of your stimulator or sales opportunities, heating from the stimulator, severe damage to the stimulator electronics and an unpleasant or jolting sensation. As a Spinal Cord Stimulation client, you should not have diathermy as possibly a remedy for the health-related ailment or as Section of a surgical course of action. Potent electromagnetic fields, such as energy generators or theft detection devices, can perhaps switch the stimulator off, or lead to unpleasant jolting stimulation. The method should not be billed while sleeping. The Spinal Twine Stimulator method may interfere with the operation of implanted sensing stimulators for example pacemakers or implanted cardiac defibrillators.

Stay clear of physically demanding action for 6 months after surgery, contact your medical doctor if there is fluid leaking out of your incision, For those who have pain, swelling or numbness within your legs or buttocks or should you fall. Make reference to the Instructions to be used offered on For added Indications for Use, contraindications information and prospective adverse consequences, warnings, and safeguards just before utilizing this products.

The Superion Indirect Decompression Procedure (IDS) is contraindicated for individuals who: have spinal anatomy that protect against implantation from the system or trigger the system to generally be unstable in situ (i.e., degenerative spondylolisthesis higher than grade 1), Cauda equina syndrome, or prior decompression or fusion on the index degree, scoliosis or spinous system fractures, osteoporosis, infection, allergy or reaction to any metal or implant or even a substantial System Mass Index. Prevent challenging activity for 6 weeks after surgery, contact your medical doctor if there is fluid leaking from the incision, Should you have pain, swelling or numbness in your legs or buttocks or in the event you fall. Refer to the Guidance for Use furnished on For added Indications for Use, contraindications details and possible adverse consequences, warnings, and safeguards before utilizing this item. Warning: U.S. Federal law restricts this machine to sale by or about the order of a doctor.

Stay clear of arduous activity for 6 months after surgery, contact your physician if there is fluid leaking from your incision, When you have pain, swelling or numbness in your legs or buttocks or should you tumble. Refer to the Directions for Use supplied on for additional Indications for Use, contraindications details and likely adverse outcomes, warnings, and precautions prior to using this product.

Warnings. For a affected person by using a cardiac pacemaker, contact the pacemaker enterprise to find out whether the pacemaker needs for being converted to mounted fee pacing during the radiofrequency course of action.

Warnings. For a affected individual which has a cardiac pacemaker, contact the pacemaker corporation to ascertain whether or not the pacemaker needs to generally be converted to set rate pacing during the and what will it involve? radiofrequency course of action.

Dependant on the period of your pain, You do not qualify for certainly one of our pain management solutions right now.

Warnings. Patients implanted with Boston Scientific Spinal Wire Stimulator Techniques without having ImageReady™ MRI Technology should not be exposed to Magnetic Resonance Imaging (MRI). Exposure to MRI may end in dislodgement from the stimulator or prospects, heating in the stimulator, intense damage to the stimulator electronics and an awkward or jolting feeling. Like a Spinal Cord Stimulation client, you should not have diathermy as either a treatment method for your health care condition or as Portion of a surgical course of action. Powerful electromagnetic fields, such as electricity turbines or theft detection techniques, can possibly switch the stimulator off, or bring about not comfortable jolting stimulation. The system should not be charged whilst sleeping. The Spinal Wire Stimulator procedure may interfere With all the operation of implanted sensing stimulators for instance pacemakers or implanted cardiac defibrillators.

Warnings: The Boston Scientific RF webpage products might induce interference with active products like neurostimulators, cardiac pacemakers, and defibrillators. Interference may well have an effect on the motion of these Energetic equipment or might problems them.

Refer to the Guidance for Use presented with Boston Scientific generators, electrodes and cannulas for probable adverse results, extra warnings and safety measures just before using these products and solutions.

Make reference to the Recommendations to be used provided with Boston Scientific generators, electrodes and cannulas for prospective adverse outcomes, further warnings and safeguards previous to using these items.

Warnings. People implanted with Boston Scientific Spinal Twine Stimulator Devices without the great site need of ImageReady™ MRI Engineering should not be exposed to Magnetic Resonance Imaging (MRI). Exposure to MRI may lead to dislodgement in the stimulator or qualified prospects, heating on the stimulator, significant damage to the stimulator electronics and an uncomfortable or jolting feeling. As being a Spinal Cord Stimulation patient, you should not have diathermy as possibly a cure for your health care issue or as Portion of a surgical method. Powerful electromagnetic fields, such as ability generators or theft detection units, can possibly turn the stimulator off, or bring about unpleasant jolting stimulation. The system should not be charged while sleeping. The Spinal Twine Stimulator system may well site interfere With all the Procedure of implanted sensing stimulators including pacemakers or implanted cardiac defibrillators.

Indications to be used: The Superion™ Indirect Decompression Program (IDS) is indicated to deal with skeletally experienced clients struggling from pain, numbness, and/or cramping in the legs (neurogenic intermittent claudication) secondary into a analysis of average degenerative lumbar spinal stenosis, with or without Quality one over here spondylolisthesis, having radiographic proof of thickened ligamentum flavum, narrowed lateral recess, and/or central canal or foraminal narrowing. The Superion™ Interspinous Spacer is indicated for anyone clients with impaired physical functionality who experience aid in flexion from symptoms of leg/buttock/groin pain, with or without back pain, who've undergone a minimum of six months of non-operative cure. The Superion Interspinous Spacer could be implanted at 1 or 2 adjacent lumbar ranges in patients in whom treatment is indicated at not more than two concentrations, from L1 to L5. Contraindications, warnings, safety measures, Unintended effects.