meddevicedb.com FDA Device Reference

ConvaVAC™ Negative Pressure Wound Therapy System

K253263 Class II Traditional
Decision Date
2026-06-24
Sponsor / Applicant
Convatec Limited, Gdc Building

Technical Specification

510(k) Submission ID K253263
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2026-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ConvaVAC™ Negative Pressure Wound Therapy System received FDA 510(k) clearance under submission number K253263, sponsored by Convatec Limited, Gdc Building. 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 2026-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.