# K071300: Modification to Smith & Nephew RF Denervation  Probes  & RF Cannulae

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew, Inc.
- Decided: Jul 20, 2007 after 72 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: 4 generations back to K870028 (1987). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K034012: Smith & Nephew RF Denervation Probes & RF Cannulae, Smith & Nephew, Inc. (2004) Summary page 1.

## Indications for use
Smith & Nephew RF Denervation Probes and RF Cannulae are indicated for use in RF heat lesion procedures for the relief of pain.

Source page: https://510kreport.com/device/K071300
Methodology: https://510kreport.com/methodology