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Spinal Frontiers · Regulatory Watch · FDA decision

Brainlab clears updated spine planning, navigation and alignment software

FDA decision · Brainlab

30 September 2026

Brainlab received 510(k) clearance for version 3.0 of its spine planning software together with its spine and trauma navigation and spinal alignment applications.

Type
FDA decision
Company
Brainlab
Device
Spine Planning 3.0; Spine & Trauma Navigation; Alignment System Spine
Date
30 September 2026
Jurisdiction
US
Classification
510(k) K262257 (OLO)
Source
FDA 510(k) database

Official source →Source checked

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