Class Class II

Rod Registration Frame (K230989)

K230989 2023-05-05 Special
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Description

Rod Registration Frame by Nu Vasive, Incorporated — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230989
Clearance Date2023-05-05
Clearance TypeSpecial
Product CodeOLO
Regulation Number882.4560

Categories

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