Class Class II

NuVasive Reline System (K223181)

K223181 2023-01-11 Traditional
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Description

NuVasive Reline System by Nu Vasive, Incorporated — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223181
Clearance Date2023-01-11
Clearance TypeTraditional
Product CodeNKB
Regulation Number888.3070

Categories

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