Class Class II

SpineLinc Anterior Cervical Implant System (K250764)

K250764 2025-12-05 Traditional
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Description

SpineLinc Anterior Cervical Implant System by Lincotek Medical, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250764
Clearance Date2025-12-05
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080

Categories

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