meddevicedb.com FDA Device Reference

Avance Abdominal Dressing Kit

K161939 Class II Traditional
Decision Date
2016-11-17
Sponsor / Applicant
Molnlycke Health Care Us, LLC

Technical Specification

510(k) Submission ID K161939
Product Code OXJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2016-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Avance Abdominal Dressing Kit received FDA 510(k) clearance under submission number K161939, sponsored by Molnlycke Health Care Us, LLC. 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 2016-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code OXJ and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.