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Smith & Nephew, Inc.
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FOOTPRINT ULTRA PK4.5MM AND 5.5MM SUTURE ANCHOR, SL is an FDA 510(k)-cleared medical device (K123579) manufactured by Smith & Nephew, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 22, 2013. Regulation: 8.