Class Class II

ARIX Humerus System (K230938)

K230938 2023-05-03 Special
Home/ Devices/ ARIX Humerus System (K230938)

Description

ARIX Humerus System by Jeil Medical Corporation — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230938
Clearance Date2023-05-03
Clearance TypeSpecial
Product CodeHRS
Regulation Number888.3030

Categories

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