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

Clearance record K201692

NuVasive Modulus XLIF Interbody System · Nu Vasive, Incorporated · decided 2020-10-29 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ModulusD1775850Nuvasive, Inc.MAX OVD PHM00195377039309