Class Class II

SternaFuse Ti Fixation System (K252661)

K252661 2025-11-19 Traditional
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Description

SternaFuse Ti Fixation System by Fusion Innovations, LLC, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252661
Clearance Date2025-11-19
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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