Half a century ago, the surgically created dialysis arteriovenous fistula (AVF) was conceived. Although the useable AVF is considered the preferred form of hemodialysis vascular access, assuming it matures sufficiently for use, persistently poor maturation rates and early failure have long signaled the need for any change that could yield improved outcomes. For a particular patient subset, that time seems to have arrived with the FDA approval of two devices that create AVF via percutaneous catheter-guided techniques. These devices function to avoid aspects of surgically created AVFs that can contribute to complications, such as poor incisional site healing and vessel clamping and dissection, as well as demonstrating superior AVF maturation, earlier cannulation, and fewer short-term complications (1-4).