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Empower H100, Cyber Ho 100, Litho 100

K180922 Class II Special
Decision Date
2018-05-08
Sponsor / Applicant
Quanta System Spa

Technical Specification

510(k) Submission ID K180922
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2018-05-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Empower H100, Cyber Ho 100, Litho 100 received FDA 510(k) clearance under submission number K180922, sponsored by Quanta System Spa. 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 2018-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.