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

XenoSure Dura Biologic Patch

K Number: K183513 · Decision Jun 13, 2019
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
42
Applicant Total
32
Review Days
177

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Basic Information

Device Name
XenoSure Dura Biologic Patch
K Number
K183513
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5910
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LeMaitre Vascular, Inc.
Date Received
December 18, 2018
Decision Date
June 13, 2019
Product Code
GXQ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GXQ Dura Substitute

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