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

Clearance record K120352

STRYKER QUIKFLAP STERILE PROCEDURE PACK · Stryker · decided 2012-06-11 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
(unnamed)12-01530SStryker Leibinger GmbH & Co. KGGWO07613252288190
(unnamed)12-01538SStryker Leibinger GmbH & Co. KGGXR07613252288237
(unnamed)12-01532SStryker Leibinger GmbH & Co. KGGWO07613252288206
(unnamed)12-01534SStryker Leibinger GmbH & Co. KGGWO07613252288213
(unnamed)12-01531SStryker Leibinger GmbH & Co. KGGWO07613252288183
(unnamed)12-01536SStryker Leibinger GmbH & Co. KGGWO07613252288220