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Power Enhanced, Robotic Assisted and/or Microprocessor Upper and Lower Extremity Rehabilitative Devices (MyoPro/IpSiHand/Motus)
Medicare Medical Policy
Origination: February 5, 2025
Review Date: May 20, 2025
Next Review: April 2026

*** This policy was implemented in the absence of National Coverage Determinations (NCD) or Local Coverage Determinations (LCD) coverage criteria. This policy applies to all Blue Medicare HMO, Blue Medicare PPO, Blue Medicare Rx members, and members of any third-party Medicare plans supported by Blue Cross NC through administrative or operational services. ***

Description of Procedure or Service

Upper extremity powered exoskeleton devices are used for chronic upper limb weakness; these custom fabricated orthotic (braces) devices are used to support, stabilize, position, and assist movement, thereby promoting functional activities of daily living. They can also use sensors on the muscles to help self-initiate movement. These devices are intended for stroke patients undergoing rehabilitation and would be included as part of prescribed physical therapy to enable stroke patients to exercise independently otherwise they would be unable to do so.

The MyoPro (Myomo) is a myoelectric powered upper extremity orthotic. This orthotic device weighs about 1.8 kilograms (4 pounds), has manual wrist articulation, and myoelectric initiated bi-directional elbow movement. The MyoPro detects weak muscle activity from the affected muscle groups. A therapist or prosthetist/orthoptist can adjust the gain (amount of assistance), signal boost, thresholds, and range of motion. Potential users include patients with traumatic brain injury, spinal cord injury, brachial plexus injury, amyotrophic lateral sclerosis, and multiple sclerosis. Use of robotic devices for therapy has been reported. The MyoPro is the first myoelectric orthotic available for home use.

IpsiHand is a brain-computer interface (BCI) device designed to help stroke survivors regain upper extremity function. It uses brain signals to control a hand-worn device, enabling patients to perform movements they might otherwise be unable to do.

Motus hand and foot devices are FDA Class 1 at-home stroke rehab robots that use high-dose repetitive task practice to help stroke survivors improve range of motion and strength of their arm(s) and/or improve walking speed, endurance, range of motion, strength and treat foot drop for overall improvement in activities of daily living.

Policy Statement

Power enhanced Robotic Assisted and/or Microprocessor Upper and Lower Extremity Devices (i.e, MyoPro, IpsiHand, Motus) are considered investigation and experimental and therefore are not covered by the plan.

Benefit Application

Please refer to the member’s individual Evidence of Coverage (EOC) for benefit determination. Coverage will be approved according to the EOC limitations if the criteria are met.

Coverage decisions will be made in accordance with:

  • The Centers for Medicare & Medicaid Services (CMS) National Coverage Determination (NCD);
  • General coverage guidelines included in Original Medicare manuals unless superseded by operational policy letters or regulations; and
  • Written coverage decisions of local Medicare (LCD, LCA) carriers and intermediaries with jurisdiction for claims in the geographic area in which services are covered.

Benefit payments are subject to contractual obligations of the Plan. If there is a conflict between the general policy guidelines contained in the Medical Coverage Policy Manual and the terms of the member’s particular Evidence of Coverage (EOC), the EOC always governs the determination of benefits.

Indications for Coverage

Myoelectric upper extremity orthotic device (e.g., MyoPro) is considered experimental, investigational, and unproven for all indications, including but not limited to use by individuals with stroke, trauma, brachial plexus injury, cerebral palsy, or any other neurological or neuromuscular disease or injury.

IpsiHand is a brain-computer interface (BCI) device is considered experimental, investigational and unproven for all indications including but not limited to use by individuals who have had a stroke.

Motus Hand and Foot devices are robotic assisted devices and are considered experimental, investigational and unproven for all indications including but not limited to use by individuals who have had a stroke.

There is insufficient literature in the peer-reviewed publications to assess safety, efficacy, long-term outcomes, or patient management associated with the use of the myoelectric upper extremity orthotic devices (e.g., MyoPro Orthosis, IpsiHand and Motus Hand and Foot) for upper extremity paralysis or paresis

Billing/Coding/Physician Documentation Information

This policy may apply to the following codes.  Inclusion of a code in the section does not guarantee reimbursement. 

Applicable codes: L8701, L8702, E0738, E0739

  • Note: Per CMS miscellaneous/unspecified codes cannot be used for billing of these devices.

References:

  1. National Coverage Determination Durable Medical Equipment Reference List 280.1 accessed on 02/06/2025 via NCD - Durable Medical Equipment Reference List (280.1)
  2. BCBSNC Corporate Medical Policy “Myoelectric Prosthetic Components for the Upper Limb” effective 8/2020; accessed via Myoelectric Prosthetic Components for the Upper Limb | Providers | Blue Cross NC on 2/6/2025
  3. Improved Disabilities Of The Arm, Shoulder And Hand Scores After Myoelectric Arm Orthosis Use At Home In Chronic Stroke: A Retrospective Study; Pub. March 21, 2024
  4. Myoelectric Arm Orthosis Assists Functional Activities: A 3 Month Home Use Outcome Report; Pub. September 2023
  5. Giving Them a Hand: Wearing a Myoelectric Elbow-Wrist-Hand Orthosis Reduces Upper Extremity Impairment in Chronic Stroke; Pub. January 25, 2017
  6. Prosthetics & Orthotics, Prosthetics Devices, & Therapeutic Shoes (CMS.gov) accessed on 02/06/25 via Prosthetics & Orthotics, Prosthetic Devices, & Therapeutic Shoes | CMS
  7. Medicare Claims Processing Manual, Chapter 20 Durable Medical Equipment, Prosthetics, Orthotics and Supplies (DMEPOS) Effective date 03/28/2024 via Medicare Claims Processing Manual, accessed on 02/06/2025

Policy Implementation/Update Information:

Revision Dates:

2/6/2025 New policy implemented. Power Enhanced, Robotic Assisted and/or Microprocessor Upper and Lower Extremity Rehabilitative Devices (MyoPro, IpsiHand and Motus)

Approval Dates:

Medical Coverage Policy Committee: April 17, 2025      

Physician Group Advisory/UM Committee: May 20, 2025

Policy Owner:  Amy Russo, LPN
Medical Policy Coordinator