Class Class II

BellaTek Bars (K241032)

K241032 2024-07-15 Traditional
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Description

BellaTek Bars by Biomet 3i, LLC — FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241032
Clearance Date2024-07-15
Clearance TypeTraditional
Product CodeNHA
Regulation Number872.3630

Categories

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