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

Clearance record K193136

Stryker Customized Mandible Recon Plate Kit · Stryker · decided 2020-03-26 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
(unnamed)78-30028Stryker Leibinger GmbH & Co. KGJEY07613252599654
(unnamed)78-31020Stryker Leibinger GmbH & Co. KGJEY07613252599661
(unnamed)78-21020Stryker Leibinger GmbH & Co. KGJEY07613252578239
(unnamed)78-20020Stryker Leibinger GmbH & Co. KGJEY07613252578222
(unnamed)78-21028Stryker Leibinger GmbH & Co. KGJEY07613252578208
(unnamed)78-31028Stryker Leibinger GmbH & Co. KGJEY07613252599678
(unnamed)78-20028Stryker Leibinger GmbH & Co. KGJEY07613252578215
(unnamed)78-30020Stryker Leibinger GmbH & Co. KGJEY07613252599647