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

Clearance record K201349

Smith+Nephew Arthroscopes · Smith & Nephew · decided 2020-07-20 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
DIRECT VIEW AND VIDEO SCOPE72205881SSmith & Nephew, Inc.HRX00885556915905
DIRECT VIEW AND VIDEO SCOPES72205880SSmith & Nephew, Inc.HRX00885556915899
DIRECT VIEW AND VIDEO SCOPE72205881Smith & Nephew, Inc.HRX00885556915882
DIRECT VIEW AND VIDEO SCOPES72205880Smith & Nephew, Inc.HRX00885556915875