POSTERIOR ANNULOPLASTY BAND (MODEL 607)

POSTERIOR ANNULOPLASTY BAND (MODEL 607) is an FDA 510(k)-cleared medical device (K960356) manufactured by The Heart Valve Div. Medtronic Cardiovascular Surg. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 1996. Regulation: 8.