# K940729: Pioneer Laboratories Bone Plate with Cerclage Cables

- Pathway: 510(k) (Traditional)
- Applicant: Pioneer Surgical Technology
- Decided: Dec 21, 1994 after 306 days
- Product code: JDQ (Cerclage, Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 3 cite it directly.
0 of 5 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
- K151716: Cable-Ready Cable Grip System: Cable-Ready Bone Plate System (2016), 1 descendant of its own
- K151888: Frontier Medical Devices In-line Orthopedic Cable Cerclage System (2015), 1 descendant of its own
- K261271: Cable-Ready® Cable Grip System (2026), 0 descendants of its own
- K153242: Frontier Medical Devices In-Line Orthopedic Cable Cerclage System (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K940729
Methodology: https://510kreport.com/methodology