Cleared Traditional

Restrata? MiniMatrix

K223725 · Acera Surgical, Inc. · General & Plastic Surgery
May 2023
Decision
156d
Days
Risk

About This 510(k) Submission

K223725 is an FDA 510(k) clearance for the Restrata? MiniMatrix, a Absorbable Synthetic Wound Dressing, submitted by Acera Surgical, Inc. (St. Louis, US). The FDA issued a Cleared decision on May 18, 2023, 156 days after receiving the submission on December 13, 2022. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K223725 FDA.gov
FDA Decision Cleared SESE
Date Received December 13, 2022
Decision Date May 18, 2023
Days to Decision 156 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code QSZ — Absorbable Synthetic Wound Dressing
Device Class
Definition Intended As A Physical Barrier To Cover The Wound And Provide A Moist Wound Environment. Intended To Be Left On Wounds After Topical Application.