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

Clearance record K183232

Double ENDOBUTTON Fixation Device · Smith and Nephew, Inc. · decided 2019-03-12 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Double ENDOBUTTON71934990Smith & Nephew, Inc.HTN HWC00885556486191
Double ENDOBUTTON71934989Smith & Nephew, Inc.HTN HWC00885556486146
Double ENDOBUTTON71935024Smith & Nephew, Inc.HTN HWC00885556467640
Double ENDOBUTTON71934993Smith & Nephew, Inc.HTN HWC00885556424544