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

Clearance record K230989

Rod Registration Frame · Nu Vasive, Incorporated · decided 2023-05-05 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
PULSE5050435Nuvasive, Inc.OLO00195377153913
PULSE5050355Nuvasive, Inc.OLO00195377153906
PULSE5050455Nuvasive, Inc.OLO00195377153937
PULSE5050348Nuvasive, Inc.OLO00195377153791
PULSE5050335Nuvasive, Inc.OLO00195377153784
PULSE5050448Nuvasive, Inc.OLO00195377153920