Class Class II

Scarlet® AL-T (K242589)

K242589 2024-10-23 Traditional
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Description

Scarlet® AL-T by Spineart SA, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242589
Clearance Date2024-10-23
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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