Class Class II

iFuse TORQ TNT™ Implant System (K241504)

K241504 2024-08-19 Traditional
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Description

iFuse TORQ TNT™ Implant System by SI-BONE, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241504
Clearance Date2024-08-19
Clearance TypeTraditional
Product CodeOUR
Regulation Number888.3040

Categories

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