# K200874: TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End

- Pathway: 510(k) (Traditional)
- Applicant: Innovasis, Inc.
- Decided: Jun 30, 2020 after 90 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: 1 generation back to K901035 (1990). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042034: Nuvasive Maxcess Light Guide, Nuvasive, Inc. (2004) Summary page 4.
- K901035: Fiber Optic Light Guide or Fiber Optic Cable, Cuda Products Co. (1990) Summary page 4.

## Indications for use
The TruView Light Cable is intended to provide surgical site illumination from a fiber optic light source.

Source page: https://510kreport.com/device/K200874
Methodology: https://510kreport.com/methodology
