Class Class II

METICULY Patient-specific titanium mesh implant (K252958)

K252958 2026-01-14 Traditional
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Description

METICULY Patient-specific titanium mesh implant by Meticuly Co., Ltd., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252958
Clearance Date2026-01-14
Clearance TypeTraditional
Product CodeGXN
Regulation Number882.5330

Categories

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