Class Class II

Estremo Fibular Nail (K250197)

K250197 2025-10-17 Traditional
Home/ Devices/ Estremo Fibular Nail (K250197)

Description

Estremo Fibular Nail by Citieffe S.R.L., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250197
Clearance Date2025-10-17
Clearance TypeTraditional
Product CodeHSB
Regulation Number888.3020

Categories

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