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

Clearance record K092812

SYNTHES (USA) 2.7MM/ 3.5MM LCP ANTEROLATERAL DISTAL TIBIA PLATES · Synthes (Usa) · decided 2010-05-11 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
LCPSD241.443Synthes GmbHHRS10886982003249
LCPSD241.445Synthes GmbHHRS10886982003287
LCPSD241.442Synthes GmbHHRS10886982003225
LCPSD241.449Synthes GmbHHRS10886982003324
LCPSD241.453Synthes GmbHHRS10886982003362
LCPSD241.444Synthes GmbHHRS10886982003263
LCPSD241.452Synthes GmbHHRS10886982003348
LCPSD241.448Synthes GmbHHRS10886982003300