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..