The Superion Indirect Decompression System (IDS) is contraindicated for patients who: have spinal anatomy that avert implantation on the product or result in the unit to get unstable in situ (i.e., degenerative spondylolisthesis larger than quality 1), Cauda equina syndrome, or prior decompression o

Contraindications. The Spinal Twine Stimulator devices aren't for sufferers who are unable to function the method, have failed trial stimulation by failing to obtain powerful pain relief, are poor surgical dangers, or are Expecting. Warnings. Individuals implanted with Boston Scientific Spina