Class Class II

Collagen Dura Regeneration Membrane – Repair (K251191)

K251191 2025-11-18 Traditional
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Description

Collagen Dura Regeneration Membrane - Repair by Collagen Matrix, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251191
Clearance Date2025-11-18
Clearance TypeTraditional
Product CodeGXQ
Regulation Number882.5910

Categories

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