# K113762: Checkmate Metatarso-Phalangeal (MTP) Arthrodesis System

- Pathway: 510(k) (Traditional)
- Applicant: Arthrosurface, Inc.
- Decided: Feb 6, 2012 after 47 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: 10 generations back to K962616 (1996). 87 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 89 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101240: Closed Fusion Plate, MTP Plate, Talus Plate, Model 824077021, 22; 824677021, 22, 824071001, 824071101, 824671001, 82467, DePuy Orthopaedics, Inc. (2010) Summary page 2.
- K052614: Low Profile Plate and Screw System, Arthrex, Inc. (2005) Summary page 2.
- K100776: Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot System, Synthes (Usa) (2010) Summary page 2.

## Most influential descendants
- K162391: AlignMATE™ Lapidus Arthrodesis System (2017), 0 descendants of its own

## Indications for use
The CheckMate TM Metatarso-Phalangeal (MTP) Arthrodesis System is intended for use in stabilization and fixation of the 1st MTP joint in the foot for fusion, osteotomy, nonunion, malunion or revision surgery.

Source page: https://510kreport.com/device/K113762
Methodology: https://510kreport.com/methodology