Back to Spinal Implants
Vertex Reconstruction
No active recall
FDA product code: KWP · Category: Appliance, Fixation, Spinal Interlaminal
Severity Snapshot
699 total reports2005-04 – 2025-03 date range3.4% physician / facility reported96.6% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
Click any bar to view those reports ↓
Top Patient Outcomes
Click any bar to view those reports ↓
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
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.
Filter by failure mode
Filter by outcome
Loading reports…