Class Class II

CurvaFix Low Profile System (K252019)

K252019 2025-08-29 Traditional
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Description

CurvaFix Low Profile System by Curvafix, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252019
Clearance Date2025-08-29
Clearance TypeTraditional
Product CodeHWC
Regulation Number888.3040

Categories

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