AOPA has recently received reports of increased RAC activity (details here) and has scheduled several educational webinars to help you prepare. The first webinar will cover the basics of what the renewed RAC audits mean for O&P providers and how to be prepared to respond to an audit request when it is received. The second webinar […]

AOPA members should be aware of proposed education standards by the Assistive Technology Professional (ATP) that could potentially encroach on the O&P profession. AOPA encourages members to make public comments about a proposed set of Assistive Technology education standards that are currently being advanced by the Rehabilitation Engineering and Assistive Technology Society of North American (RESNA). The […]

As a result of the series of meetings during the Policy Forum involving Senator Kerrey and top members of the Senate and the Finance Committee, and particularly through AOPA Past President Tom Watson’s intercession with Senate Majority Leader McConnell, important language relating to the July 2015 draft LCD was inserted into the Committee report which […]

In 2013, AOPA, in conjunction with the American Podiatric Medical Association (APMA) and the Pedorthic Footcare Association (PFA), developed a joint statement on the interpretation of HCPCS codes L3000, L3010, L3020, and L3030.  The joint statement was presented to AOPA leadership at the time and was approved for publication.  On May 13, 2016 a follow […]

AOPA has recently received reports of increased Recovery Audit Contractor (RAC) activity focusing on the provision of ankle foot orthoses, especially in Jurisdiction A and Jurisdiction D. While the existing RAC contractors have been authorized to begin new audits for some time now, pending the competition for and award of the single, national DMEPOS RAC […]

On May 10, 2016, the Food and Drug Administration (FDA) released a document entitled, Technical Considerations for Additive Manufactured Devices: Draft Guidance for Industry and Food and Drug Administration Staff.  The publication of this document marks the first foray of the FDA into potential regulation of devices that use additive manufacturing as a means of […]

In January of 2016, new authority granted to CMS to build on DME competitive bidding to set pricing more broadly and nationally took effect. This authority allows CMS to use pricing established as a result of competitive bidding programs for specific DME products in certain parts of the country to be applied more broadly to […]

Noridian, who serves as the Jurisdiction D Durable Medical Equipment Medicare Administrative Contractor (DME MAC), has released the most recent quarterly results of its ongoing pre-payment review of claims for several codes. For AFOs described by HCPCS codes L1960, L1970 and L4360: from December 2015 through March 2016, a total of 1008 claims were reviewed; […]