Class Class II

ARx® SAI Implant System (K241464)

K241464 2024-07-29 Traditional
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Description

ARx® SAI Implant System by Life Spine, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241464
Clearance Date2024-07-29
Clearance TypeTraditional
Product CodeOUR
Regulation Number888.3040

Categories

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