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

MONET Anterior Cervical Interbody Fusion Cage System with Supplementary Fixation Plate

K Number: K182151 · Decision Oct 11, 2018
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
14
Review Days
64

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Basic Information

Device Name
MONET Anterior Cervical Interbody Fusion Cage System with Supplementary Fixation Plate
K Number
K182151
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ctl Medical Corporation
Date Received
August 8, 2018
Decision Date
October 11, 2018
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Similar 510(k) Clearances

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

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Other Clearances by Ctl Medical Corporation

K Number Device Name
K233947 KLIMT™ Expandable Lumbar Interbody Fusion (LIF) Cage System
K231715 MONDRIAN™ Anterior Lumbar Plate System
K231359 RODIN™ Expandable Lumbar Cage System
K220513 NITRO Interbody Fusion Cage System Family
K220334 MONET Anterior Cervical Plate System
K211785 CASSATT™ SIJ Fixation System
K213641 MONDRIAN ALIF Cage with Supplementary Fixation Plate
K213491 Universal Pilot Guidance Instrument System
K192863 MONDRIAN Lumbar Interbody Fusion Cage System
K172788 MONET™ Anterior Cervical Interbody Fusion Cage System
Search all 14 clearances from Ctl Medical Corporation →