Cleared Special

ACELL MATRISTEM WOUND SHEET

K092926 · Acell, Inc. · General & Plastic Surgery
Oct 2009
Decision
35d
Days
Risk

About This 510(k) Submission

K092926 is an FDA 510(k) clearance for the ACELL MATRISTEM WOUND SHEET, a Wound Dressing With Animal-derived Material(s), submitted by Acell, Inc. (Columbia, US). The FDA issued a Cleared decision on October 28, 2009, 35 days after receiving the submission on September 23, 2009. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K092926 FDA.gov
FDA Decision Cleared SESE
Date Received September 23, 2009
Decision Date October 28, 2009
Days to Decision 35 days
Submission Type Special
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

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