# K232780: CC-Clip® Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Cc-Instruments, Inc.
- Decided: Dec 18, 2023 after 98 days
- Product code: HTN (Washer, Bolt Nut)
- 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: 7 generations back to K792022 (1979). 40 ancestors in all.
No later device cites it as a predicate yet.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052776: Tightrope Acromioclavicular (AC) Device, Titanium, Stainless Steel , Models AR-2257, AR-TBD, Arthrex, Inc. (2005) Summary page 6.

## Indications for use
The CC-Clip® device is intended as an adjunct in coracoclavicular ligament disruption repair. Specifically, the CC-Clip® device is intended to provide fixation during the healing process following a syndesmotic trauma, such as fixation of acromioclavicular separations due to coracoclavicular ligament disruptions.

Source page: https://510kreport.com/device/K232780
Methodology: https://510kreport.com/methodology