Class Class II

PressON Spinal Fixation System (K253331)

K253331 2025-10-14 Special
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK253331
Clearance Date2025-10-14
Clearance TypeSpecial
Product CodeNKB
Regulation Number888.3070

Categories

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