# K010612: Vectorvision Knee

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: Sep 6, 2001 after 189 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.
838 later devices descend from it; 5 cite it directly.
3 of 839 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
- K021306: Vectorvision CT-Free Knee (2002), 387 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
- K121498: Percunav (2012), 222 descendants of its own

Source page: https://510kreport.com/device/K010612
Methodology: https://510kreport.com/methodology