# K171293: G3™ Active Plate® Miniature System

- Pathway: 510(k) (Traditional)
- Applicant: Genesis Fracture Care, Inc.
- Decided: Oct 23, 2017 after 174 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- 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 K962616 (1996). 109 ancestors in all.
No later device cites it as a predicate yet.
0 of 110 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061748: Fragment Plate System, Hand Innovations, LLC (2006) Summary page 5.
- K141527: Depuy Synthes Variable Angle Locking Hand System, Synthes USA (2015) Summary page 5.
- K083364: 2.5 MM Multidirectional Threaded Pegs, Models 131211110-131211130, 1.5 MM Locking Screws, Models 131220408-131220424, DePuy Orthopaedics, Inc. (2008) Summary page 5.
- K051605: Sbi K-Wires, Small Bone Innovations, LLC (2005) Summary page 5.
- K132895: WMT Implantable K-Wire, Wrightmedicaltechnologyinc (2013) Summary page 5.

## Indications for use
The G3™ Active Plate® Miniature System is intended for fracture fixation in patients 18 years of age and older requiring stabilization of mal-unions, non-unions, osteotomies and repair of closed and open fractureV in small bones. The system is indicated for the fixation of small bone fractures including, but not limited to, fractures of the hand, foot, wrist and ankle.

Source page: https://510kreport.com/device/K171293
Methodology: https://510kreport.com/methodology