Liberty SI Lateral Implant System— 510(k) K231923

Substantially Equivalent

Spinal Simplicity, LLC

FDA 510(k) clearance K231923 for Liberty SI Lateral Implant System, Substantially Equivalent on 2023-12-05. Applicant: Spinal Simplicity, LLC.

Clearance details

Applicant: Spinal Simplicity, LLC
Product code: Code OUR
Advisory panel: Orthopedic
Date received: 2023-06-30
Decision date: 2023-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OUR

product code OUR

Death: 3
Injury: 347
Total: 350

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.