← Product Code [GXI](/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GXI) · K001588

# ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, ARTHROCARE SYSTEM 20 (K001588)

_Arthrocare Corp. · GXI · Aug 17, 2000 · Neurology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GXI/K001588

## Device Facts

- **Applicant:** Arthrocare Corp.
- **Product Code:** [GXI](/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GXI.md)
- **Decision Date:** Aug 17, 2000
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 882.4725
- **Device Class:** Class 2
- **Review Panel:** Neurology

## Regulatory Identification

A radiofrequency lesion probe is a device connected to a radiofrequency (RF) lesion generator to deliver the RF energy to the site within the nervous system where a lesion is desired.

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**Source:** [https://fda.innolitics.com/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GXI/K001588](https://fda.innolitics.com/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GXI/K001588)

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