Class Class II

Spine Navigation System (K233725)

K233725 2024-07-26 Traditional
Home/ Devices/ Spine Navigation System (K233725)

Description

Spine Navigation System by Medivis, Inc. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233725
Clearance Date2024-07-26
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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