meddevicedb.com FDA Device Reference

Surgical laser fibers

K200234 Class II Special
Decision Date
2020-02-25
Sponsor / Applicant
Quanta System Spa

Technical Specification

510(k) Submission ID K200234
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2020-02-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Surgical laser fibers received FDA 510(k) clearance under submission number K200234, 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 2020-02-25.

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.