Cleared Traditional

Geistlich Wound Matrix PLUS

K213607 · Geistlich Pharma AG · General & Plastic Surgery
Apr 2022
Decision
164d
Days
Risk

About This 510(k) Submission

K213607 is an FDA 510(k) clearance for the Geistlich Wound Matrix PLUS, a Wound Dressing With Animal-derived Material(s), submitted by Geistlich Pharma AG (Wolhusen, Lu, CH). The FDA issued a Cleared decision on April 28, 2022, 164 days after receiving the submission on November 15, 2021. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K213607 FDA.gov
FDA Decision Cleared SESE
Date Received November 15, 2021
Decision Date April 28, 2022
Days to Decision 164 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code KGN — Wound Dressing With Animal-derived Material(s)
Device Class

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