Advanced LumFix Spinal Fixation System— 510(k) K222229

Substantially Equivalent

CG Bio Co., Ltd.

FDA 510(k) clearance K222229 for Advanced LumFix Spinal Fixation System, Substantially Equivalent on 2023-05-25. Applicant: CG Bio Co., Ltd..

Clearance details

Applicant: CG Bio Co., Ltd.
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2022-07-25
Decision date: 2023-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hwaseong-Si, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code NKB

product code NKB

Death: 27
Injury: 5,033
Malfunction: 4,140
Total: 9,200

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.