Class Class II

NEXUS® Hip Stem (K250444)

K250444 2025-05-15 Traditional
Home/ Devices/ NEXUS® Hip Stem (K250444)

Description

NEXUS® Hip Stem by Microport Orthopedics, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250444
Clearance Date2025-05-15
Clearance TypeTraditional
Product CodeLZO
Regulation Number888.3353

Categories

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