# K132797: L'DISQ

- Pathway: 510(k) (Traditional)
- Applicant: U&I Corporation
- Decided: Jul 30, 2014 after 327 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)
- K010811: Perc-D Spinewand, Arthrocare Corp. (2001)
- K030954: Arthrocare Percd Spinewand, Arthrocare Corp. (2003) Summary page 1.
- K053447: Arthrocare Perc-D Spinewand, Arthrocare Corp. (2005) Summary page 1.
- K061259: Modification to Arthrocare Perc-D Spinewand, Arthrocare Corp. (2006) Summary page 1.

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

## Indications for use
The LDISQ®& is indicated for coagulation and ablation of disc material to treat symptomatic patients with contained herniated discs.

Source page: https://510kreport.com/device/K132797
Methodology: https://510kreport.com/methodology