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

Clearance record K201569

CUVIS-spine · Curexo, Inc. · decided 2021-05-19 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
(unnamed)CUVIS-spineCUREXO, Inc.OLO08800043830006