
Smith & Nephew, Inc.
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SMITH & NEPHEW FOOTPRINT RCX PK SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K093935) 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 April 4, 2010. Regulation: 8.