# K143716: DSM Biomedical DPR Cable

- Pathway: 510(k) (Traditional)
- Applicant: Dsm Biomedical
- Decided: Oct 29, 2015 after 304 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
Longest line of descent: 1 generation back to K920201 (1992). 1 ancestor in all.
7 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K920201: Titanium Alloy Songer Cable System, Sofamor Danek Mfg., Inc. (1992) Summary page 4.

## Most influential descendants
- 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
- K243344: Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage Sutures (2025), 0 descendants of its own

## Indications for use
The DPR Cable is intended for: Spinal applications include sublaminar and intraspinous process wiring for trauma applications. Trochanteric reattachment after trochanteric osteotomy following total hip arthroplasty. Sternotomy indications including the “rewiring” of osteomized sternums. Trauma surgery indications including olecranon, ankle, patella and some shoulder fracture rewiring. The device is intended for single patient use only.

Source page: https://510kreport.com/device/K143716
Methodology: https://510kreport.com/methodology