# K201677: Arthrex Mesh Plates

- Pathway: 510(k) (Traditional)
- Applicant: Arthrex, Inc.
- Decided: Sep 2, 2020 after 75 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: 12 generations back to K962616 (1996). 101 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 104 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170547: Arthrex Mesh Plate System, Arthrex, Inc. (2017) Summary page 4.
- K143702: Arthrex Blunt Tip Screws with Fiber Tape, Arthrex, Inc. (2015) Summary page 4.

## Most influential descendants
- K203834: Arthrex Patella SuturePlates (2021), 1 descendant of its own
- K240487: EVOS Patella Plates (2024), 0 descendants of its own

## Indications for use
The Arthrex Mesh Plates are intended for use in stabilization of fresh fractures, revision procedures, osteotomies, joint fusion and reconstruction of small bones and bone fragments of the hand/wrist, foot/ankle, osteopenic bone and patella fractures.

Source page: https://510kreport.com/device/K201677
Methodology: https://510kreport.com/methodology