Class Class II

OnPoint Augmented Reality Spine System (K241870)

K241870 2024-08-19 Special
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Description

OnPoint Augmented Reality Spine System by Onpoint Surgical, Inc. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241870
Clearance Date2024-08-19
Clearance TypeSpecial
Product CodeSBF
Regulation Number882.4560

Categories

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