NuVasive Cohere ALIF System Intervertebral Body Fusion Device— 510(k) K221751

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K221751 for NuVasive Cohere ALIF System Intervertebral Body Fusion Device, Substantially Equivalent on 2022-10-21. Applicant: Nu Vasive, Incorporated.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code OVD
Advisory panel: Orthopedic
Date received: 2022-06-16
Decision date: 2022-10-21
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.