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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K153186

Adjustable Fixation Device · Arthrocare Corp. · decided 2016-01-28 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ULTRABUTTON72290003Smith & Nephew, Inc.MBI00885556613825