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

ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System

K Number: K220115 · Decision May 13, 2022
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
24
Review Days
119

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Basic Information

Device Name
ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System
K Number
K220115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MiRus, LLC
Date Received
January 14, 2022
Decision Date
May 13, 2022
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 MiRus, LLC

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K232481 RIGEL™ 3DR Anterior Cervical Corpectomy System
K232154 MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation
K230369 EUROPA™ Navigated Instruments
K220441 CYGNUS™ MoRe Anterior Cervical Plate System
K210800 IO Expandable Lumbar Interbody Fusion System
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