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ATLANTIS® Anterior Cervical Plate System 7200023Recalls & reported problems

Medtronic Sofamor Danek, Inc. · PLATE 7200023 ATL VISION ELITE 23MM · Class 2 · Implant

All models of ATLANTIS Anterior Cervical Plate System (46)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00613994625199), received between Jan 13, 2017 and Jan 13, 2017 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Swelling1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 13, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT ON (B)(6) 2015, PATIENT HAD A FUSION DONE AT LEVEL C6-7. PER OP NOTES, SCREWS WERE PLACED IN C6-7. HERNIATED DISK MATERIAL WAS REMOVED FROM TOP OF NERVE ROOT. A 7 MM GRAFT WAS COUNTER SUNK IN POSITION AT C6-7. A PLATE AFTER THIS WAS PLACED WITH 13 MM SCREWS. NO INTRAOPERATIVE COMPLICATIONS WERE REPORTED. POST-OP, PATIENT HAD SWELLING AROUND THE AREA WHERE THE SPINE SURGERY WAS PERFORMED.

    Patient problems: Swelling

    MAUDE report 6248740 ↗

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Sources and updates

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