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

Impulse Interbody Fusion System

K Number: K201287 · Decision Dec 22, 2020
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
16
Review Days
222

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Basic Information

Device Name
Impulse Interbody Fusion System
K Number
K201287
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
May 14, 2020
Decision Date
December 22, 2020
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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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
K213918 DeGen Navigated Instrumentation
K213901 Cyclops™ Anterior Cervical Plate System
K210090 Impulse AM Interbody Fusion System
K203816 DeGen Navigated Instrumentation
Search all 16 clearances from Degen Medical →