# K063244: Arc Surgical Bone Reduction Screw

- Pathway: 510(k) (Traditional)
- Applicant: Arc Surgical, LLC
- Decided: Dec 27, 2006 after 62 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: 2 generations back to K961498 (1997). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023294: Bosworth Coraco-Clavicular Screw, Howmedica Osteonics Corp. (2002) Summary page 1.
- K792022: Herbert Bone Screw, Zimmer, Inc. (1979) Summary page 1.
- K013775: Twinfix Interfragmentary Compression Screw System, Stryker Leibinger (2002) Summary page 1.
- K984209: Stainless Steel Taper Foreman Nail Cannulated Screw, Stainless Steel Cannulated Screw, Short Thread, Stainless Steel Ped, Biomet, Inc. (1999) Summary page 1.

## Most influential descendants
- K111608: Slic Screw Repair System (2011), 0 descendants of its own

## Indications for use
The bone reduction screw is intended to provide fixation and anatomically reduce two bones or bone portions. Specifically, these indications include scapholunate ligament repair, scapholunate reduction, lunotriquetral ligament repair, lunotriquetral reduction, and carpal instability.

Source page: https://510kreport.com/device/K063244
Methodology: https://510kreport.com/methodology