MEMO 3D SEMIRIGID ANNULOPLASTY RING

MEMO 3D SEMIRIGID ANNULOPLASTY RING is an FDA 510(k)-cleared medical device (K071327) manufactured by Sorin Biomedica Cardio S.R.L.. 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 9, 2007. Regulation: 8.