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FDA 510(k) Applications Submitted by THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980534
02/11/1998
DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608H
THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
K960356
01/25/1996
POSTERIOR ANNULOPLASTY BAND (MODEL 607)
THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
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