Class Class II

HILINE™ Fixation System (K230565)

K230565 2023-04-20 Traditional
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Description

HILINE™ Fixation System by Globus Medical, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230565
Clearance Date2023-04-20
Clearance TypeTraditional
Product CodeOWI
Regulation Number888.3010

Categories

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