# K935481: Sponger Cable System, Modification

- Pathway: 510(k) (Traditional)
- Applicant: Pioneer Surgical Technology
- Decided: Jan 26, 1994 after 125 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.
81 later devices descend from it; 9 cite it directly.
0 of 82 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
- K993286: Pioneer Silicoat Sternal Cable (1999), 64 descendants of its own
- K051165: KLS Martin Sternal Talon (2006), 62 descendants of its own
- K070169: KLS Martin Quick Disc, Sternal Talon and Sternal Plating - Sterile (2007), 61 descendants of its own
- K122293: Pioneer Sternal Cable Plate System (2012), 46 descendants of its own
- K151983: KLS Martin LSS Plating System (2016), 45 descendants of its own

Source page: https://510kreport.com/device/K935481
Methodology: https://510kreport.com/methodology