K241367
- 510(k) number
- K241367
- Device name
- RF Cannula
- Applicant
- Shanghai Samedical & Plastic Instruments Co., Ltd. CN
- Product code
- GXI — Probe, Radiofrequency Lesion
- Decision date
- 2025-01-23
- Date received
- 2024-05-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K241367.pdf
Official FDA record: K241367
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.