meddevicedb.com FDA Device Reference

Thermage CPT System and Accessories

K173759 Class II Special
Decision Date
2018-01-08
Sponsor / Applicant
Solta Medical

Technical Specification

510(k) Submission ID K173759
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2018-01-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Thermage CPT System and Accessories received FDA 510(k) clearance under submission number K173759, sponsored by Solta Medical. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2018-01-08.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.