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

DeGen Navigated Instrumentation

K Number: K213918 · Decision Feb 9, 2022
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
16
Review Days
56

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Basic Information

Device Name
DeGen Navigated Instrumentation
K Number
K213918
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Degen Medical
Date Received
December 15, 2021
Decision Date
February 9, 2022
Product Code
OLO
Advisory Committee
Neurology
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
OLO Orthopedic Stereotaxic Instrument

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Other Clearances by Degen Medical

K Number Device Name
K251829 DeGen Medical Patient Specific Implant (PSI) System
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
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 →