Class Class II

PressON Spinal Fixation System (K223529)

K223529 2023-05-02 Traditional
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Description

PressON Spinal Fixation System by Nexus Spine, LLC — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223529
Clearance Date2023-05-02
Clearance TypeTraditional
Product CodeNKB
Regulation Number888.3070

Categories

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