Class Class II

Q Guidance System; Mako Spine System; (K241517)

K241517 2024-08-27 Traditional
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Description

Q Guidance System; Mako Spine System; by Stryker Leibinger GmbH & Co KG — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241517
Clearance Date2024-08-27
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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