Class Class II

DeGen Medical Patient Specific Implant (PSI) System (K251829)

K251829 2025-12-08 Traditional
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Description

DeGen Medical Patient Specific Implant (PSI) System by Degen Medical, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251829
Clearance Date2025-12-08
Clearance TypeTraditional
Product CodeOVD
Regulation Number888.3080

Categories

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