# K201662: REDUCT® Headless Compression Screw System

- Pathway: 510(k) (Special)
- Applicant: Skeletal Dynamics, Inc.
- Decided: Jul 16, 2020 after 27 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
Longest line of descent: 3 generations back to K030302 (2003). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143624: Headless Compression Screw System, Skeletal Dynamics, LLC (2015) Summary page 4.

## Most influential descendants
- K220723: Hand Trauma Screw System (2022), 1 descendant of its own
- K230908: Hand Trauma Threaded Nail System (2023), 0 descendants of its own

## Indications for use
The Skeletal Dynamics REDUCT® Headless Compression Screw System is intended for fixation of osseous fragments or fractures, arthrodesis of small joints, and osteotomies, with the appropriately sized screw.

Source page: https://510kreport.com/device/K201662
Methodology: https://510kreport.com/methodology