Cleared Traditional

K180051 - XSTAT 30, 1-Pack (FDA 510(k) Clearance)

May 2018
Decision
130d
Days
Class 2
Risk

K180051 is an FDA 510(k) clearance for the XSTAT 30, 1-Pack. This device is classified as a Non-absorbable, Expandable, Hemostatic Sponge For Temporary Internal Use (Class II - Special Controls, product code PGZ).

Submitted by Revmedx, Inc. (Wilsonville,, US). The FDA issued a Cleared decision on May 18, 2018, 130 days after receiving the submission on January 8, 2018.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4452. To Control Bleeding In Junctional, Non-compressible Wounds Until Surgical Care Is Acquired..

Submission Details

510(k) Number K180051 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 2018
Decision Date May 18, 2018
Days to Decision 130 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code PGZ - Non-absorbable, Expandable, Hemostatic Sponge For Temporary Internal Use
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4452
Definition To Control Bleeding In Junctional, Non-compressible Wounds Until Surgical Care Is Acquired.