# K071745: Baylis Pain Management Single-Use Probe

- Pathway: 510(k) (Special)
- Applicant: Baylis Medical Co., Inc.
- Decided: Jul 19, 2007 after 22 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 K002389 (2000). 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)
- K002389: Baylis Pain Management Probe/PMP-20-145 and Baylis Pain Management Connector Cable/PMX-Bay-Bay, Baylis Medical Co., Inc. (2000) Summary page 1.

## Indications for use
Baylis Pain Management Single-Use Probe will be used in conjunction with a Baylis Pain Management Connector Cable and the Baylis Pain Management Generator to create radiofrequency lesions in nervous tissue.

Source page: https://510kreport.com/device/K071745
Methodology: https://510kreport.com/methodology