Advanced Bone Plate— 510(k) K221150

Substantially Equivalent

Double Medical Technology, Inc.

FDA 510(k) clearance K221150 for Advanced Bone Plate, Substantially Equivalent on 2023-01-25. Applicant: Double Medical Technology, Inc..

Clearance details

Applicant: Double Medical Technology, Inc.
Product code: Code HRS
Advisory panel: Orthopedic
Date received: 2022-04-20
Decision date: 2023-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Xiamen, CN

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.