05/29/2026
One year ago, the Spur® Peripheral Retrievable Stent System received FDA De Novo Clearance.
Today, we celebrate more than a regulatory milestone.
Received during NCVH 2025, the clearance marked a defining moment for Reflow Medical.
Over the past year, that milestone has become momentum: growing clinical adoption, expanding scientific evidence, and continued focus on progress in BTK disease treatment.
We are deeply grateful to our clinical partners and to the Reflow Medical team who made this journey possible. Your trust, insight, commitment, and persistence continue to help bring Spur closer to the patients who need it most.
Here’s to one year of FDA De Novo Clearance and to building on this momentum together.