K240340
- 510(k) number
- K240340
- Device name
- Surgical Drive System (Model: ES70, ES90, E8)
- Applicant
- Guangdong Jinme Medical Technology Co., Ltd. CN
- Product code
- DZI — Drill, Bone, Powered
- Decision date
- 2024-07-18
- Date received
- 2024-02-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K240340.pdf
Official FDA record: K240340
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.