# K191009: Arsenal Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Trilliant Surgical
- Decided: Aug 12, 2019 after 118 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: 15 generations back to K962616 (1996). 110 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 113 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983495: Syntec-Taichung Non-Sterile Bone Plate and Screw Implants, Model#'S 222020-248120, 240050-240980, 241130-246620, 4240420, Syntec Scientific Corp. (1998) Summary page 4.
- K131445: Osteomed Extremilock Foot Plating System, Osteomed LP (2013) Summary page 4.
- K160177: Gridlock Ankle Plating System, Trilliant Surgical, Ltd. (2016) Summary page 4.
- K130964: Gridlock Plating System, Trilliant Surgical, Ltd. (2013) Summary page 4.

## Most influential descendants
- K212378: Arsenal Ankle Plating System (2022), 0 descendants of its own
- K200062: Foot and Ankle System (2021), 0 descendants of its own

## Indications for use
The Arsenal Plating System is intended for use in trauma and reconstructive procedures of the small bones in the hand/foot, ankle, and other bones appropriate for the size of the device. The plates (implants), screws (implants), washers (implants), olive wires (instruments), and guide wires (instruments) are intended for single use only.

Source page: https://510kreport.com/device/K191009
Methodology: https://510kreport.com/methodology