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

EUROPA™ Posterior Cervical Fusion System

K Number: K242516 · Decision Nov 19, 2024
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
24
Review Days
88

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Basic Information

Device Name
EUROPA™ Posterior Cervical Fusion System
K Number
K242516
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MiRus, LLC
Date Received
August 23, 2024
Decision Date
November 19, 2024
Product Code
NKG
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
NKG Posterior Cervical Screw System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NKG), ordered by most recent decision date.

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Other Clearances by MiRus, LLC

K Number Device Name
K253444 EUROPA™ Posterior Cervical Fusion Navigated Instruments
K252733 ATLAS™ Expandable Osteotomy Wedge System
K241175 MiRus MoRe Lumbar Plating System
K232348 RIGEL™ 3DR Standalone Anterior Cervical Interbody Fusion System
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
K220115 ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System
K210800 IO Expandable Lumbar Interbody Fusion System
Search all 24 clearances from MiRus, LLC →