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M6-C 7LRecalls & reported problems

Spinal Kinetics, Inc. · Artificial Cervical Disc, 7L (7mm H x 17mm W x 14mm D) · Class 3 · Implant

Data updated Oct 16, 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 00812388030070), received between Sep 6, 2023 and Sep 6, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Collapse” (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 16, 2026.

Most reported problems

Device problems

  • Collapse1
  • Material Disintegration1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • InjurySep 6, 2023Collapse; Material Disintegration; Collapse; Material Disintegration

    INFORMATION PROVIDED STATES THAT HAD M6-C IMPLANTED AT C5/6 & C6/7 IN (B)(6) 2016. DURING A CONTROL APPOINTMENT LYSIS WAS SEEN ON THE X-RAY AND DISC HEIGHT REDUCTION ON THE M6-C AT THE C5/6 LEVEL. THE PATIENT HAD NO SYMPTOMS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17695659 ↗

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Sources and updates

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