# K942906: Agee-Wristjack Pre-Drill Kit

- Pathway: 510(k) (Traditional)
- Applicant: Hand Biomechanics Lab, Inc.
- Decided: Dec 22, 1994 after 184 days
- Product code: HTW (Bit, Drill)
- Device class: 1
- Regulation: 21 CFR 888.4540
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K984498: Synthes (Usa) Articulating Distal Radius (Adrf) System (1999), 5 descendants of its own
- K012294: Wristore Fixator (2002), 3 descendants of its own
- K042761: Wristore Distal Radius Fracture Fixator, 4600 Series (2004), 1 descendant of its own
- K101338: Newfix External Fixation System (2011), 0 descendants of its own
- K052498: Fragment Specific Fixator (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K942906
Methodology: https://510kreport.com/methodology