Class Class II

Triathlon® Hinge Knee System; Triathlon® Revision Insert X3® (K230416)

K230416 2023-05-19 Traditional
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Description

Triathlon® Hinge Knee System; Triathlon® Revision Insert X3® by Stryker — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230416
Clearance Date2023-05-19
Clearance TypeTraditional
Product CodeKRO
Regulation Number888.3510

Categories

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