NuVasive Modulus ALIF System— 510(k) K230894

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K230894 for NuVasive Modulus ALIF System, Substantially Equivalent on 2023-06-16. Applicant: Nu Vasive, Incorporated.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code OVD
Advisory panel: Orthopedic
Date received: 2023-03-31
Decision date: 2023-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OVD

product code OVD

Death: 5
Injury: 495
Total: 500

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.