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

DSM Biomedical Porcine Pericardium Dental Membrane

K Number: K160474 · Decision Jun 7, 2016
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
56
Applicant Total
7
Review Days
109

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Basic Information

Device Name
DSM Biomedical Porcine Pericardium Dental Membrane
K Number
K160474
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kensey Nash Corporation Dba Dsm Biomedical
Date Received
February 19, 2016
Decision Date
June 7, 2016
Product Code
NPL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NPL Barrier, Animal Source, Intraoral

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K Number Device Name
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K170245 DSM Biomedical Dental Bone Graft
K141738 MEDEOR MATRIX WOUND DRESSING
K133169 MESO TENDON MATRIX
K132025 MESO BILAYER SURGICAL MESH