Class Class II

PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System (K222381)

K222381 2023-04-27 Traditional
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Description

PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System by Stryker GmbH — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222381
Clearance Date2023-04-27
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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