Class Class II

Juliet® Ti LL Lumbar Interbody Device (K241321)

K241321 2024-07-18 Traditional
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Description

Juliet® Ti LL Lumbar Interbody Device by Spineart SA — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241321
Clearance Date2024-07-18
Clearance TypeTraditional
Product CodeOVD
Regulation Number888.3080

Categories

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