FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DeGen Medical Patient Specific Implant (PSI) System

K Number: K251829 · Decision Dec 8, 2025
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
16
Review Days
178

Basic Information

Device Name
DeGen Medical Patient Specific Implant (PSI) System
K Number
K251829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Degen Medical
Date Received
June 13, 2025
Decision Date
December 8, 2025
Product Code
OVD
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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Other Clearances by Degen Medical

K Number Device Name
K252737 DeGen Medical Latitude-C AM Cervical Interbody Fusion System
K250667 DeGen Medical Patient Specific Implant (PSI) System
K241077 DeGen Medical Patient Specific Implant (PSI) System
K231199 Solar Lumbar Interbody Fusion System
K223418 DeGen Impulse AM™ System
K213918 DeGen Navigated Instrumentation
K213901 Cyclops™ Anterior Cervical Plate System
K210090 Impulse AM Interbody Fusion System
K203816 DeGen Navigated Instrumentation
K201287 Impulse Interbody Fusion System
Search all 16 clearances from Degen Medical →