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Cook Biotech Incorporated
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BIODESIGN SURGISIS ANTERIOR POSTERIOR PELVIC FLOOR GRAFTS is an FDA 510(k)-cleared medical device (K130006) manufactured by Cook Biotech Incorporated. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on April 4, 2013. Regulation: 8.

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