Class Class II

Companion Spine DIAM™ Instrumentation (K253118)

K253118 2025-12-16 Traditional
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Description

Companion Spine DIAM™ Instrumentation by Companion Spine France, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253118
Clearance Date2025-12-16
Clearance TypeTraditional
Product CodeQLR
Regulation Number888.4520

Categories

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