XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter

XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter is an FDA 510(k)-cleared medical device (K221986) manufactured by Transit Scientific, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 17, 2022. Regulation: 8.