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Medtronic Reusable Instruments

MEDTRONIC SOFAMOR DANEK, INC. · Model EX0113026 · UDI-DI 00643169325944

HXW Prescription
3
510(k) clearances
320
Adverse events
3
Recalls
224
Facilities

Description

RIGHT EX0113026 CORONAL PLANE BENDER

Recalls

DateFirmReason
2021-06-30Aesculap Implant Systems LLCCustomized coronal rod benders may deform the implant when used with the spinal system devices.
2021-06-30Aesculap Implant Systems LLCCustomized coronal rod benders may deform the implant when used with the spinal system devices.
2014-12-15Synthes, Inc.Certain lots have the potential for tip breakage while bending 2.0 mm thick plates. If device is used and breaks while in the Operating Room, surgical delay may occur while altern

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.