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

Clearance record K230716

Robotic Graft Delivery Instruments · Medtronic Sofamor Danek, Inc. · decided 2023-07-18 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Robotic Graft Delivery InstrumentsRBT060001MEDTRONIC SOFAMOR DANEK, INC.OLO00763000708559
Robotic Graft Delivery InstrumentsRBT060002MEDTRONIC SOFAMOR DANEK, INC.OLO00763000708566