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

Clearance record K122742

NUVASIVE BENDINI SPINAL ROD BENDING SYSTEM · Nuvasive, Inc. · decided 2012-12-07 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Bendini8210010Nuvasive, Inc.OLO00887517094698
Bendini2040001Nuvasive, Inc.OLO00887517172532