Class Class II

OsteoCentric Navigated Instruments System (K250520)

K250520 2025-10-27 Traditional
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Description

OsteoCentric Navigated Instruments System by Osteocentric Technologies, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250520
Clearance Date2025-10-27
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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