Class Class II

Fine Osteotomy™ (K253300)

K253300 2025-10-28 Special
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK253300
Clearance Date2025-10-28
Clearance TypeSpecial
Product CodeHRS
Regulation Number888.3030

Categories

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