# K010968: Vectorvision CT/Fluoro

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: Aug 30, 2001 after 150 days
- Product code: HAW (Neurological Stereotaxic Instrument)
- Device class: 2
- Regulation: 21 CFR 882.4560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
225 later devices descend from it; 4 cite it directly.
3 of 226 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K042721: Kolibri Spine (2005), 187 descendants of its own
- K053159: Vectorvision Spine (2006), 155 descendants of its own
- K024192: Vectorvision FLUORO3D (2003), 144 descendants of its own
- K070106: VV Fluoro 3D (2007), 119 descendants of its own
- K062086: Navivision (2006), 77 descendants of its own

Source page: https://510kreport.com/device/K010968
Methodology: https://510kreport.com/methodology