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CMF SpinaLogic®

CMF SpinaLogic is a portable, battery-powered, micro-controlled, noninvasive bone growth stimulator indicated as an adjunct electromagnetic treatment to primary lumbar spinal fusion surgery for one or two levels. It has the following benefits:

  • Lightweight and comfortable
  • Easy to use
  • Can be used after anterior or posterior approach in fusion surgery
  • Noninvasive
  • Requires simple, one-button operation
  • Device is worn for only 30 minutes per day

This treatment has been shown in pre-clinical studies to help the body's own healing process begin working. Clinical studies have also shown that individuals who use CMF SpinaLogic after fusion surgery showed a 21 percentage point increase in healing over those who did not.

CONTRAINDICATIONS : Demand-type pacemaker and implantable cardioverter defibrillator (ICD) may be adversely-affected by exposure to combined static and dynamic magnetic fields. Physicians should not prescribe CMF SpinaLogic for patients with such devices. The safety and effectiveness of CMF SpinaLogic in pregnant women have not been studied, and the effect of the device on the mother or the developing fetus are unknown, thus, this device should not be used in pregnant women. If a woman becomes pregnant during treatment with CMF SpinaLogic, treatment should be discontinued immediately.

PRECAUTIONS : The safety and effectiveness of the use of this device on individuals lacking skeletal maturity have not been established.

The safe and effectiveness of this device in treating patients with the following conditions have not been established and therefore the safety and effectiveness of the device in these individuals are unknown: osseous and ligamentous spinal trauma, spondylitis, Paget's disease, severe osteoporosis, metastatic cancer, renal disease, and uncontrolled diabetes mellitus. Animal studies conducted to date so not suggest any long term effects from use of this device. However, long term effects in humans are unknown. Compliance with the treatment schedule, timely battery change and proper care of the device are essential.The device will not perform properly and treatment may be unnecessarily prolonged if the patient fails to adhere to the care routine. This device should not be used if there are mental or physical conditions which preclude patient compliance with the physician and device instructions.

ADVERSE EFFECTS : No known significant adverse effects have resulted from the use of this device. Clinical studies, animal studies, and tissue culture experiments conducted with the CMF SpinaLogic Bone Growth Stimulator magnetic fields have not indicated any evidence of significant adverse effects.

CAUTION : USA Law restricts these devices to sale by or on the order of a physician.

  • Specifications
  • Technical specifications
  • Product Manuals/IFUs
  • Brand Documents


Ordering Information

Part Number Description
01-207-0007 CMF SpinaLogic


Part Number Description
11-1520 Soft Goods Kit
11-9102 Extension Belt
25-100-0049 Batteries

Technical specifications



Product Manuals/IFUs

Patient Manual:
pdf EN |

Brand Documents