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American Medical Systems, Inc.
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AMS ELEVATE ANTERIOR & APICAL PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE is an FDA 510(k)-cleared medical device (K082677) manufactured by American Medical Systems, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 22, 2008. Regulation: 8.

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