Class Class II

Q Interbody Instruments (K252873)

K252873 2026-02-06 Traditional
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Description

Q Interbody Instruments by K2m,Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252873
Clearance Date2026-02-06
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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