
Smith & Nephew, Inc.
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Smith & Nephew TRUCLEAR ULTRA Mini Tissue Removal Device is an FDA 510(k)-cleared medical device (K161763) manufactured by Smith & Nephew, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 21, 2016. Regulation: 8.

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