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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K053371
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Recall
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FDA Recall
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AdVance"Male Sling System, REF 720088-01 & AdVance" XP Male Sling System REF 720163-01 (not commer... 2 12/16/2014 American Medical Systems, Inc.
AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling System (US) 720088-02 AMS AdVance... 2 11/07/2012 American Medical Systems, Inc.
Model # 720088-01: AMS AdVance Male Sling System, US; Model # 720088-02: AMS AdVance Male Sling Syst... 2 12/27/2010 American Medical Systems, Inc.
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