Class Class II

ProLift Micro Expandable Spacer System (K223430)

K223430 2023-05-04 Traditional
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Description

ProLift Micro Expandable Spacer System by Life Spine, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223430
Clearance Date2023-05-04
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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