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

Clearance record K170977

SURESHOT Distal Targeting System V4.0 Trauma Interface · Smith & Nephew, Inc. · decided 2017-05-03 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
TRIGEN71692857Smith & Nephew, Inc.OLO00885556584675
TRIGEN71692852Smith & Nephew, Inc.OLO00885556584644