meddevicedb.com FDA Device Reference

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider

K162751 Class II Traditional
Decision Date
2017-05-01
Sponsor / Applicant
Surgical Instrument Services and Savings, Inc.

Technical Specification

510(k) Submission ID K162751
Product Code NUJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2017-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider received FDA 510(k) clearance under submission number K162751, sponsored by Surgical Instrument Services and Savings, Inc.. 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 2017-05-01.

Classification & Regulation

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