Class Class II

Atlas Spine Project X Expandable Posterior Lumbar Interbody System (K251969)

K251969 2025-08-15 Traditional
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Description

Atlas Spine Project X Expandable Posterior Lumbar Interbody System by Atlas Spine, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251969
Clearance Date2025-08-15
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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