Class Class II

Activmotion S (K241539)

K241539 2024-07-30 Traditional
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Description

Activmotion S by Newclip Technics — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241539
Clearance Date2024-07-30
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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