Class Class II

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System (K253748)

K253748 2026-01-23 Traditional
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Description

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System by Life Spine, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253748
Clearance Date2026-01-23
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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