meddevicedb.com FDA Device Reference

Distal Elbow Plating System

K231623 Class II Traditional
Decision Date
2023-08-28
Sponsor / Applicant
Skeletal Dynamics, Inc.

Technical Specification

510(k) Submission ID K231623
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2023-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Distal Elbow Plating System received FDA 510(k) clearance under submission number K231623, sponsored by Skeletal Dynamics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.