Class Class II

Dakota LP System (K250769)

K250769 2025-11-24 Traditional
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Description

Dakota LP System by Precision Spine, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250769
Clearance Date2025-11-24
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080

Categories

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