# K101496: Cablecap Model: WLF, STZ, Acm

- Pathway: 510(k) (Traditional)
- Applicant: Sensormed
- Decided: Sep 14, 2010 after 105 days
- Product code: FST (Light, Surgical, Fiberoptic)
- Device class: 2
- Regulation: 21 CFR 878.4580
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K042034 (2004). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082992: Axxion Light Guide, Spinal Elements, Inc. (2009) Summary page 1.

## Most influential descendants
- K113330: Cablecap (2012), 0 descendants of its own

## Indications for use
The CableCap device attaches to the distal end of high intensity light cables. The device absorbs and diffuses the light transmitted through the cable in order to prevent p~atient burns and igniting-flammable items in the surgidal suite. It is necessary to check each light cable to determine which CableCap model (STZ, ACM, WLF) to use. See product instructions for cleaning and sterilization protocols. The device is not intended to be used to illuminate the surgical field.

Source page: https://510kreport.com/device/K101496
Methodology: https://510kreport.com/methodology