Class Class II

Fine Osteotomy™ (K231314)

K231314 2023-06-02 Special
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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) NumberK231314
Clearance Date2023-06-02
Clearance TypeSpecial
Product CodePBF
Regulation Number888.3030

Categories

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