# K091118: Foot and Hand Motion System

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Dec 16, 2009 after 243 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.
31 later devices descend from it; 4 cite it directly.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K121277: Z-Snap Off Screw, Z-Double Thread Compression Screw, Z-Guide Wire, Z-Staple (2012), 24 descendants of its own
- K131061: Restore Bunion Correction System (2013), 15 descendants of its own
- K170214: Additive Orthopaedics Locking Lattice Plate (2017), 8 descendants of its own
- K222645: Treace Medical Concepts (TMC) Implant Fixation System (2022), 6 descendants of its own
- K183011: Additive Orthopaedics Patient Specific 3D Locking Lattice Plates (2019), 5 descendants of its own

## Indications for use
The implants of the Foot and Hand Motion System are indicated for the fixation of bone fractures and for bone reconstruction in the hand and forefoot surgery.

Source page: https://510kreport.com/device/K091118
Methodology: https://510kreport.com/methodology
