Class Class II

iFuse Bedrock Granite Implant System (K253094)

K253094 2025-10-09 Special
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Description

iFuse Bedrock Granite Implant System by SI-BONE, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253094
Clearance Date2025-10-09
Clearance TypeSpecial
Product CodeOUR
Regulation Number888.3040

Categories

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