Class Class II

Fine Osteotomy™ (K241356)

K241356 2024-09-05 Traditional
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Description

Fine Osteotomy™ by Bodycad Laboratories, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241356
Clearance Date2024-09-05
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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