Class Class II

LumiVy™ Lumbar IBF System (K223412)

K223412 2023-01-06 Special
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Description

LumiVy™ Lumbar IBF System by Vy Spine, LLC — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223412
Clearance Date2023-01-06
Clearance TypeSpecial
Product CodeMAX
Regulation Number888.3080

Categories

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