Class Class II

Anatase Spine Surgery Navigation System (K230783)

K230783 2023-04-21 Special
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Description

Anatase Spine Surgery Navigation System by Remex Medical Corp. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230783
Clearance Date2023-04-21
Clearance TypeSpecial
Product CodeOLO
Regulation Number882.4560

Categories

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