# K920201: Titanium Alloy Songer Cable System

- Pathway: 510(k) (Traditional)
- Applicant: Sofamor Danek Mfg., Inc.
- Decided: Apr 8, 1992 after 84 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.
10 later devices descend from it; 3 cite it directly.
0 of 11 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
- K143716: DSM Biomedical DPR Cable (2015), 7 descendants of its own
- K170206: Arthrex FiberTape Cerclage (2017), 5 descendants of its own
- K232755: Arthrex FiberTape and TigerTape Cerclage Sutures (2023), 2 descendants of its own
- K230976: Arthrex Radiopaque FiberTape Cerclage sutures (2023), 1 descendant of its own
- K260018: Arthrex FiberButton (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K920201
Methodology: https://510kreport.com/methodology