Class Class II

OsteoFlo HydroFiber (K251720)

K251720 2025-07-02 Special
Home/ Devices/ OsteoFlo HydroFiber (K251720)

Description

OsteoFlo HydroFiber by SurGenTec, LLC, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251720
Clearance Date2025-07-02
Clearance TypeSpecial
Product CodeMQV
Regulation Number888.3045

Categories

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