Updates on Spur® Retrievable Scaffold Therapy (RST) at AMP
At the Amputation Prevention Symposium (AMP) held in Chicago in August, S. Jay Mathews, MD, provided an excellent review: “Retrievable Stent Therapy for CLTI: update on the DEEPER REVEAL Trial” (NCT05358353). Thomas Zeller, MD’s outstanding presentation covered “Retrievable Scaffold Therapy in conjunction with DCB for Infrapopliteal Arterial Disease: Two-year Results of the DEEPER OUS Study” (NCT04162418).
Read the latest clinical trial news
Dr. Lorenzo Patrone Discusses Spur RST in Singapore
Learn more about Retrievable Scaffold Therapy (RST)
New Scientific Advisory Board Member
We are delighted to welcome Sean Lyden, MD to the world-renowned Scientific Advisory Board here at Reflow Medical. Dr. Lyden leads a team of over 30 physicians in Ohio and Florida as Chairman of Vascular Surgery at Cleveland Clinic. He is also an active researcher and author who serves on various boards.
Walking for P.A.D. Patients, Caregivers and Providers
Team Reflow stepped up to the Light-A-Red-Candle challenge this summer, walking in support of The Way to My Heart campaign to raise awareness of peripheral artery disease (PAD). Reflow is a partner of the Global PAD Association, a 501(c)(3) nonprofit operating as The Way to My Heart.
Visit The Way to My Heart’s site
Standout Presentations at CIRSE 2024
Dr. Andrew Holden, Dr. Michael Lichtenberg, and Dr. Mahmood Razavi gave well-attended presentations on the topic, Spur RST: maximizing BTK CLTI treatment outcomes, and Dr. Holden also shared two-year results of the DEEPER OUS study (NCT04162418) at CIRSE 2024 in Lisbon, Portugal in September.
“Doctor Radio” Interview with Reflow CEO Isa Rizk
Dr. Todd Berland, a Vascular Specialist who hosts the “Vascular Surgery Show” on Sirius/XM’s Doctor Radio, interviewed Reflow’s CEO Isa Rizk on July 19 about the company’s Spur Retrievable Scaffold Therapy.
Peripheral Product Certification Progress
We marked another milestone on the road to enabling commercialization of our full portfolio of peripheral products in the EU and globally. The Wingman™ CTO Crossing Catheter, the Spex®, and the Spex® LP Shapeable Support Microcatheters are now certified under the EU Medical Device Regulations (2017/745).
Q4 ‘24 Conferences
