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CD Horizon
No active recall
FDA product code: KWP · Category: Appliance, Fixation, Spinal Interlaminal
Severity Snapshot
7,807 total reports1996-09 – 2026-03 date range3.1% physician / facility reported96.9% manufacturer reported6 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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