The Superion™ Interspinous Spacer is indicated for those sufferers with impaired physical perform who knowledge relief in flexion from symptoms of leg/buttock/groin pain, with or without the need of back pain, which have undergone not less than 6 months of non-operative cure. The Superion Interspinous Spacer may very well be implanted at 1 or 2 adjacent lumbar levels in sufferers in whom cure is indicated at not more than two ranges, from L1 to L5.

Stay clear of arduous activity for six weeks after surgery, contact your doctor if there is fluid leaking from a incision, if you have pain, swelling or numbness in your legs or buttocks or should you fall. Confer with the Guidance for Use delivered on for additional Indications for Use, contraindications information and potential adverse consequences, warnings, and precautions just before using this merchandise.

Prevent strenuous exercise for 6 weeks after surgery, contact your medical professional if there is fluid leaking out of your incision, When you have pain, swelling or numbness within your legs or buttocks or should you fall. Make reference to the Guidelines for Use furnished on for additional Indications to be used, contraindications data and probable adverse results, warnings, and safeguards before applying this merchandise.

The Superion™ Interspinous Spacer is indicated for the people clients with impaired physical purpose who working experience aid in flexion from symptoms of leg/buttock/groin pain, with or devoid of back pain, who've been through at least 6 months of non-operative remedy. The Superion Interspinous Spacer could be implanted at one or two adjacent lumbar concentrations in clients in whom cure is indicated at no more than two levels, from L1 to L5.

Warnings. People implanted with Boston Scientific Spinal Wire Stimulator Devices with no ImageReady™ MRI Technologies should not be exposed to Magnetic Resonance Imaging (MRI). Publicity to MRI may well end in dislodgement of your stimulator or sales opportunities, heating from the stimulator, serious harm to the stimulator electronics and an awkward or jolting sensation. As a Spinal Wire Stimulation affected person, you should not have diathermy as both a remedy to get a healthcare condition or as Element of a surgical method. Potent electromagnetic fields, for instance ability generators or theft detection units, can perhaps flip the stimulator off, or lead to not comfortable jolting stimulation. The program should not be billed while sleeping. The Spinal Twine Stimulator procedure may perhaps interfere Together with the Procedure of implanted sensing stimulators for example pacemakers or implanted cardiac defibrillators.

Recommend your medical professional that you've got a Spinal Wire Stimulator in advance of under-going with other implantable system therapies so that health-related decisions is often created and appropriate basic safety actions taken. People employing therapy that generates paresthesia should not operate motorized autos such as automobiles or likely unsafe machinery and devices Using the stimulation on. here Stimulation need to be turned off first in these cases. For therapy that will not produce paresthesia (i.e. subperception therapy) it can be not as likely that unexpected stimulation changes causing distraction could occur although obtaining stimulation on when running transferring motor vehicles, equipment, and tools. Your medical doctor might be go here able to supply added information on the Boston Scientific Spinal Twine Stimulator devices. For finish indications to be used, contraindications, warnings, safeguards, and Unwanted side effects, get in touch with 866.360.4747 or pay a visit to Pain.com.

Make reference to the Guidelines for Use delivered with Boston Scientific generators, electrodes and cannulas for prospective adverse results, extra warnings and precautions prior to applying these products.

Depending on the length of your respective pain, You do not qualify for certainly one of our pain management options at this time.

The Superion™ Interspinous Spacer is indicated for the people people with impaired physical function who practical 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 treatment. The Superion Interspinous Spacer may be implanted at a few adjacent lumbar concentrations in clients in whom treatment is indicated at not more than two degrees, from L1 visit to L5.

Make reference to the Instructions to be used delivered with Boston Scientific turbines, electrodes and cannulas for likely adverse effects, extra warnings and safety measures previous to employing these merchandise.

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The Superion™ Interspinous Spacer is indicated for the people clients with impaired physical perform who experience relief in flexion from symptoms of leg/buttock/groin pain, with or without the need of back pain, that have gone through at least 6 months of non-operative remedy. The Superion Interspinous Spacer may be implanted at a few adjacent lumbar amounts in people in whom therapy is indicated at no more than two stages, from L1 to L5.

Explore more about different sorts of treatment as well as Medical practitioners who will try and help you handle your pain.

Indications for Use: The Superion™ Indirect Decompression Technique (IDS) is published here indicated to take care of skeletally experienced people struggling from pain, numbness, and/or cramping within the legs (neurogenic intermittent claudication) secondary to some prognosis of reasonable degenerative lumbar spinal stenosis, with or devoid of Quality 1 spondylolisthesis, obtaining radiographic evidence of thickened ligamentum flavum, narrowed lateral recess, and/or central canal or foraminal narrowing. The Superion™ Interspinous Spacer is indicated for the people clients with impaired physical purpose who encounter relief in flexion from symptoms of leg/buttock/groin pain, with or with out back pain, who've undergone a minimum of six months of non-operative cure. The Superion Interspinous Spacer may very well be implanted at a couple of adjacent lumbar ranges in individuals in whom treatment is indicated at not more than two stages, from L1 to L5. Contraindications, warnings, precautions, Unwanted side effects.