# K223762: Smith & Nephew ACCORD™ Cable System

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew
- Decided: May 30, 2023 after 166 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K844068 (1985). 20 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993106: Smith & Nephew Bone Plate System (Bone Plates, Bone Screws and Accessories), Smith & Nephew, Inc. (1999) Summary page 4.
- K031162: Smith & Nephew Orthopaedic Cabling System, Smith & Nephew, Inc. (2003) Summary page 4.

## Most influential descendants
- K233949: ACCORD Cable System (2024), 0 descendants of its own

## Indications for use
The Smith & Nephew Cabling System of the Smith & Nephew ACCORD™ Cable System is indicated for general orthopaedic repair procedures including patellar fractures, general cerclage, trochanteric reattachment, femoral and tibial fractures, prophylactic banding, olecranon fractures, ankle fractures, fixation of spiral fractures in conjunction with intramedullary nail and screw fixation techniques. Trochanteric reattachment whenever the trochanter is osteotomized in any of the procedures listed below. • Primary total hip arthroplasty. • Revision total hip arthroplasty. • Any procedure using anterolateral or lateral approaches. The ACCORD™ Titanium Plates of the Smith & Nephew ACCORD™ Cable System are indicated for adult or pediatric patients as indicated for pelvic, small, and long bone fracture fixation. Indications for use include fractures of the tibia, fibula, femoral condyle, pelvis, acetabulum, metacarpals, metatarsals, humerus, ulna, middle hand and middle foot bones; treatment of the calcaneal; hip arthrodesis, and provisional hole fixation.

Source page: https://510kreport.com/device/K223762
Methodology: https://510kreport.com/methodology