Class Class II

Tibia and Fibula System (K213059)

K213059 2023-01-27 Traditional
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Description

Tibia and Fibula System by Auxein Medical Private Limited — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213059
Clearance Date2023-01-27
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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