# K170012: Foot and Hand Motion

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Apr 24, 2017 after 111 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: 11 generations back to K954385 (1996). 78 ancestors in all.
No later device cites it as a predicate yet.
0 of 79 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091118: Foot and Hand Motion System, Newclip Technics (2009) Summary page 4.
- K052576: Sbi Autofix, Small Bone Innovations, LLC (2005) Summary page 4.
- K051323: Merete Twistcut Snap-Off Bone Screw, Merete Medical GmbH (2005) Summary page 4.
- K160617: Large Screws Range, Newclip Technics (2016) Summary page 4.
- K161448: Footmotion Plating System, Newclip Technics (2016) Summary page 4.

## Indications for use
The implants of the Foot and Hand Motion are intended for the fixation of bone fractures and osteotomies, and for arthrodeses of the foot and hand in adults.

Source page: https://510kreport.com/device/K170012
Methodology: https://510kreport.com/methodology