Class Class II

Suture Button Repair System (K240835)

K240835 2024-07-19 Traditional
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Description

Suture Button Repair System by Skeletal Dynamics, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240835
Clearance Date2024-07-19
Clearance TypeTraditional
Product CodeMBI
Regulation Number888.3040

Categories

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