meddevicedb.com FDA Device Reference

Ultrasonic Osteotomy Surgical System

K201274 Class II Traditional
Decision Date
2021-02-19
Sponsor / Applicant
Smtp Technology Co., Ltd.

Technical Specification

510(k) Submission ID K201274
Product Code JDX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4580
Decision Date 2021-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ultrasonic Osteotomy Surgical System received FDA 510(k) clearance under submission number K201274, sponsored by Smtp Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2021-02-19.

Classification & Regulation

This clearance is catalogued under FDA product code JDX and 21 CFR 888.4580, within the Orthopedic review panel as a Class II device.