Class Class II

HyperFlex® Bunion Correction System (K252997)

K252997 2025-12-11 Traditional
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Description

HyperFlex® Bunion Correction System by Hyperflex Medical, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252997
Clearance Date2025-12-11
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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