Class Class II

WRISTAR MultiAx Distal Radius Kit (K252959)

K252959 2025-11-12 Traditional
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Description

WRISTAR MultiAx Distal Radius Kit by Intrauma S.P.A, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252959
Clearance Date2025-11-12
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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