IXOS Radius Plate System— 510(k) K171624

Substantially Equivalent

Stuckenbrock Medizintechnik GmbH

FDA 510(k) clearance K171624 for IXOS Radius Plate System, Substantially Equivalent on 2018-03-29. Applicant: Stuckenbrock Medizintechnik GmbH.

Clearance details

Applicant: Stuckenbrock Medizintechnik GmbH
Product code: Code HRS
Advisory panel: Orthopedic
Date received: 2017-06-02
Decision date: 2018-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tuttlingen, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.