Diamondback 360 Peripheral Orbital Atherectomy System

Diamondback 360 Peripheral Orbital Atherectomy System is an FDA 510(k)-cleared medical device (K150732) manufactured by Cardiovascular Systems, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 12, 2015. Regulation: 8.