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United States · Bill · S

S. 948 (113th)

Ensuring Access to Quality Complex Rehabilitation Technology Act of 2013

referredUnited States· United States Congress· EN

Introduced

14 May 2013

Last action

14 May 2013 · Introduced

Status

Read twice and referred to the Committee on Finance.

Sponsors

Charles Schumer, Rep. Cochran, Thad [R-MS-4], Roger Wicker, Patty Murray, Kirsten Gillibrand, Rep. Nelson, Bill [D-FL-11], Sen. Stabenow, Debbie [D-MI], Sen. Pryor, Mark L. [D-AR], Richard Durbin, Sen. Vitter, David [R-LA], Sen. Landrieu, Mary L. [D-LA], Lisa Murkowski, Sen. McCaskill, Claire [D-MO], Susan Collins, Sen. Begich, Mark [D-AK], Michael Bennet, Sen. Blunt, Roy [R-MO], Jeff Merkley, Richard Blumenthal, Christopher Murphy, Rep. Cardin, Benjamin L. [D-MD-3], Christopher Coons

Subjects

Healthcare

Source updated

20 January 2026

Healthcare

Summary

Ensuring Access to Quality Complex Rehabilitation Technology Act of 2013 - Amends title XVIII (Medicare) of the Social Security Act to cover, as medical and other health services, complex rehabilitation technology items designed and configured for a specific qualified individual to meet that individual's unique: (1) medical, physical, and functional needs related to a medical condition; and (2) capacities for basic activities of daily living (ADLs) and instrumental ADLs. Directs the Secretary of Health and Human Services (HHS) to: (1) designate complex rehabilitation technology items (excluding adaptive equipment to operate motor vehicles or certain prosthetic devices and orthotics), and (2) establish eligibility criteria for them. Prescribes requirements for payments for CRT items. Directs the Secretary to establish standards for clinical conditions for CRT item payment as well as quality standards for suppliers of such items. Directs the Secretary to establish a Healthcare Procedure Coding System (HCPCS) coding subset that uses specified HCPCS codes for CRT items. Requires payment for replacement of a CRT item (or any part of one), without regard to certain continuous use or useful lifetime restrictions established for items of durable medical equipment (DME), if a qualified ordering practitioner determines that a replacement item (or part) is necessary.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 14 May 2013

    Introduced

    Read twice and referred to the Committee on Finance.

    Source: IntroReferral

  2. 14 May 2013

    Introduced

    Introduced in Senate

    Source: IntroReferral

Votes

No vote records are attached yet.

Versions

Documents

3 official files

Sponsors

Related records

Sources

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