NuVasive Reline Cervical System— 510(k) K213654

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K213654 for NuVasive Reline Cervical System, Substantially Equivalent on 2022-02-23. Applicant: Nu Vasive, Incorporated.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code NKG
Advisory panel: Orthopedic
Date received: 2021-11-19
Decision date: 2022-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NKG

product code NKG

Death: 15
Injury: 1,090
Malfunction: 529
Total: 1,634

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.