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

Clearance record K191996

BC Reflex Uni Knee System · Bodycad Laboratories, Inc. · decided 2019-12-05 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
BC Reflex Uni018-001Laboratoires Bodycad IncHSX00688346000061
BC Reflex Uni 018-001Laboratoires Bodycad IncHSX00688346002072