VYRSA Technologies develops sacroiliac joint fusion implants for minimally invasive treatment of chronic SI joint pain. Its V1 system, now called Nevro1, uses integrated lateral transfixation with deployable titanium anchors and became FDA 510(k)-cleared for SI joint fusion in 2022. The company also developed NevroPro, a custom allograft implant designed specifically for the SI joint and offered in multiple sizes for variable anatomy.
FDA 510(k) Clearance
Compliance program