# K241367: RF Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Shanghai Samedical & Plastic Instruments Co., Ltd.
- Decided: Jan 23, 2025 after 254 days
- Product code: GXI (Probe, Radiofrequency Lesion)
- Device class: 2
- Regulation: 21 CFR 882.4725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K112231 (2011). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112231: LCCS Insulated Spinal Needle (RF Cannula), Lccs Products Limited (2011) Summary page 5.

## Indications for use
The RF cannula is intended for use in RF heat lesion procedures for the relief of pain.

Source page: https://510kreport.com/device/K241367
Methodology: https://510kreport.com/methodology