# K003589: Vectorvision Cranial, Vectorvision Spinal, Vectorvision Ent

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: May 21, 2001 after 182 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.
882 later devices descend from it; 7 cite it directly.
12 of 883 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
- K014256: Kolibri Igs Systems (2002), 419 descendants of its own
- K020631: IPLAN (2002), 343 descendants of its own
- K040050: Instatrak System with Multiple Dataset Navigation, Model IT3500 (2004), 280 descendants of its own
- K053610: Abaris (2006), 278 descendants of its own
- K012448: Vectorvision Trauma (2002), 251 descendants of its own

Source page: https://510kreport.com/device/K003589
Methodology: https://510kreport.com/methodology