CBT Screw Fixation System— 510(k) K181824

Substantially Equivalent

U&I Corporation

FDA 510(k) clearance K181824 for CBT Screw Fixation System, Substantially Equivalent on 2018-12-13. Applicant: U&I Corporation.

Clearance details

Applicant: U&I Corporation
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2018-07-09
Decision date: 2018-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Uijeongbu-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.