Cleared Traditional

PuraStat

K242634 · 3-D Matrix Europe SAS · Gastroenterology & Urology
Jan 2025
Decision
134d
Days
Risk

About This 510(k) Submission

K242634 is an FDA 510(k) clearance for the PuraStat, a Protective Coating, Mucoadhesive Application, For The Rectal Mucosa, submitted by 3-D Matrix Europe SAS (Caluire Et Cuire, FR). The FDA issued a Cleared decision on January 15, 2025, 134 days after receiving the submission on September 3, 2024. This device falls under the Gastroenterology & Urology review panel.

Submission Details

510(k) Number K242634 FDA.gov
FDA Decision Cleared SESE
Date Received September 03, 2024
Decision Date January 15, 2025
Days to Decision 134 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code PHN — Protective Coating, Mucoadhesive Application, For The Rectal Mucosa
Device Class
Definition Mucoadhesive Application For The Protective Coating Of The Rectal Mucosa.