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

Collagen Dura Regeneration Membrane - Repair

K Number: K251191 · Decision Nov 18, 2025
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
42
Applicant Total
47
Review Days
215

Basic Information

Device Name
Collagen Dura Regeneration Membrane - Repair
K Number
K251191
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5910
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Collagen Matrix, Inc.
Date Received
April 17, 2025
Decision Date
November 18, 2025
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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