meddevicedb.com FDA Device Reference

LigaSure Exact Dissector, Nano-coated

K173281 Class II Traditional
Decision Date
2018-03-02
Sponsor / Applicant
Covidien

Technical Specification

510(k) Submission ID K173281
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2018-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LigaSure Exact Dissector, Nano-coated received FDA 510(k) clearance under submission number K173281, sponsored by Covidien. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2018-03-02.

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.