# K023294: Bosworth Coraco-Clavicular Screw

- Pathway: 510(k) (Special)
- Applicant: Howmedica Osteonics Corp.
- Decided: Oct 9, 2002 after 7 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
220 later devices descend from it; 2 cite it directly.
0 of 221 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K052776: Tightrope Acromioclavicular (AC) Device, Titanium, Stainless Steel , Models AR-2257, AR-TBD (2005), 217 descendants of its own
- K112437: Arthrex Fracture System (2011), 91 descendants of its own
- K123241: Arthrex Fracture Plates (2013), 71 descendants of its own
- K082095: Ultraslide Acromioclavicular and Syndesmotic Repair Device (2008), 59 descendants of its own
- K112111: Acu-Sinch Repair System and Acumed Suture Anchor (2011), 49 descendants of its own

## Indications for use
The Bosworth Coraco-Clavicular Screw is intended for uses in cases of acromioclavicular reduction and acromioclavicular fixation; acromioclavicular reduction; coracoclavicular ligament repair, and coracoclavicular fixation; a combination of the aforementioned indications; distal clavicle extension; and muscle transfers.

Source page: https://510kreport.com/device/K023294
Methodology: https://510kreport.com/methodology