Anteralign Spinal System with Titan nanoLock Surface technology 46261060Recalls & reported problems
Medtronic Sofamor Danek, Inc. · NANO SPACER 46261060 T 6DG 20W 10X7.9X60 · Class 2 · Implant
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 00763000128500), received between Dec 2, 2022 and Dec 2, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (1 report).
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
- Migration1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 2, 2022Migration; Migration
INFORMATION WAS RECEIVED FROM A HEALTHCARE PROFESSIONAL VIA A MANUFACTURER REPRESENTATIVE REGARDING A PATIENT WITH LATERAL FUSION TH ERAPY. IT WAS REPORTED THAT THE CAGE MIGRATED SEVERELY, CAGE DOES NOT APPEAR TO HAVE TEETH TO PREVENT BACKING OUT. PATIENT HAD PAIN AND REVISION SURGERY WAS PERFORMED TO EXPLANT THE CAGE & REPLACED WITH PIVOX CAGE.
Patient problems: Pain
MAUDE report 15902802 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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