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American Medical Systems
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AMS ELEVATE PC APICAL AND POSTERIOR ( AND ANTERIOR AND APICAL) PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE is an FDA 510(k)-cleared medical device (K111118) manufactured by American Medical Systems. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 30, 2011. Regulation: 8.

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