meddevicedb.com FDA Device Reference

XSTAT 30 Pouch

K210676 Class II Traditional
Decision Date
2021-08-27
Sponsor / Applicant
Revmedx, Inc.

Technical Specification

510(k) Submission ID K210676
Product Code PGZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4452
Decision Date 2021-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XSTAT 30 Pouch received FDA 510(k) clearance under submission number K210676, sponsored by Revmedx, 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 2021-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code PGZ and 21 CFR 878.4452, within the General, Plastic Surgery review panel as a Class II device.