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

Clearance record K201756

Reprocessed MyoSure Tissue Removal Device, Reprocessed MyoSure REACH Tissue Removal Device, Reprocessed MyoSure LITE Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device for Fluent · Stryker Sustainability Solutions · decided 2020-09-25 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
(unnamed)N/ASTRYKER SUSTAINABILITY SOLUTIONS, INC.HIH07613327507102
(unnamed)N/ASTRYKER SUSTAINABILITY SOLUTIONS, INC.HIH07613327507126
(unnamed)N/ASTRYKER SUSTAINABILITY SOLUTIONS, INC.HIH07613327507133
(unnamed)N/ASTRYKER SUSTAINABILITY SOLUTIONS, INC.HIH07613327507140
(unnamed)N/ASTRYKER SUSTAINABILITY SOLUTIONS, INC.HIH07613327507119