Synthetic Bone Graft Particulate— 510(k) K241186

Name: FDA 510(k) clearance K241186
Creator: U.S. Food and Drug Administration
Published: 2025-02-21

Substantially Equivalent

Shenzhen Dazhou Medical Technology Co., Ltd.

FDA 510(k) clearance K241186 for Synthetic Bone Graft Particulate, Substantially Equivalent on 2025-02-21. Applicant: Shenzhen Dazhou Medical Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Dazhou Medical Technology Co., Ltd.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2024-04-29
Decision date: 2025-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.