# K132099: Arthrocare Coblator IQ DLR Spinewand, Arthrocare Coblator IQ DLG Spinewand

- Pathway: 510(k) (Traditional)
- Applicant: ArthroCare Corporation
- Decided: Aug 22, 2013 after 45 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K010811 (2001). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100353: Spinewand Surgical Device, Arthrocare Corp. (2010) Summary page 2.

## Most influential descendants
- K150915: Spinaut-P (2016), 0 descendants of its own

## Indications for use
The ArthroCare Coblator IQ Perc-D Spine Wands (Coblator IQ DLR and Coblator IQ DLG SpineWands) are indicated for ablation, coagulation, and decompression of disc material to treat symptomatic patients with contained herniated lumbar and lumbosacral discs. The Wands are designed to be used exclusively with the ArthroCare Coblator IQ Controller.

Source page: https://510kreport.com/device/K132099
Methodology: https://510kreport.com/methodology