Class Class II

EUROSCREW NG; EUROSCREW TCP NG (K230394)

K230394 2023-05-12 Traditional
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Description

EUROSCREW NG; EUROSCREW TCP NG by Teknimed — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230394
Clearance Date2023-05-12
Clearance TypeTraditional
Product CodeMAI
Regulation Number888.3030

Categories

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