FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MatriStem UBM Pericardial Patch

K Number: K191734 · Decision Nov 22, 2019
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
10
Applicant Total
20
Review Days
147

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Basic Information

Device Name
MatriStem UBM Pericardial Patch
K Number
K191734
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3470
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acell, Inc.
Date Received
June 28, 2019
Decision Date
November 22, 2019
Product Code
PSQ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PSQ Intracardiac Patch Or Pledget, Biologically Derived

Similar 510(k) Clearances

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Other Clearances by Acell, Inc.

K Number Device Name
K241706 MicroMatrix® UBM Particulate
K241724 Cytal® Wound Matrix; Cytal® Burn Matrix
K230980 MicroMatrix® Flex
K192725 Cytal Wound Matrix 3-Layer
K182259 Gentrix Surgical Matrix, Gentrix Surgical Matrix Hiatal
K180776 Cytal Wound Particulate
K172399 MicroMatrix
K170763 Gentrix Surgical Matrix Thick; Gentrix Surgical Matrix Extend
K162554 Gentrix Surgical Matrix
K153754 MicroMatrix
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