Class Class II

NuVasive Modulus-C Interbody System (K223731)

K223731 2023-01-12 Special
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Description

NuVasive Modulus-C Interbody System by Nuvasive, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223731
Clearance Date2023-01-12
Clearance TypeSpecial
Product CodeODP
Regulation Number888.3080

Categories

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