Class Class II

Phantom Fibula Nail System (K234128)

K234128 2024-08-22 Traditional
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Description

Phantom Fibula Nail System by Paragon 28, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK234128
Clearance Date2024-08-22
Clearance TypeTraditional
Product CodeHSB
Regulation Number888.3020

Categories

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