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

MONDRIAN ALIF Cage with Supplementary Fixation Plate

K Number: K213641 · Decision Sep 15, 2022
Classifications
1
FEI Numbers
422
Registration Numbers
422
Same Product Code
869
Applicant Total
14
Review Days
301

Basic Information

Device Name
MONDRIAN ALIF Cage with Supplementary Fixation Plate
K Number
K213641
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
November 18, 2021
Decision Date
September 15, 2022
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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K Number Device Name
K233947 KLIMT™ Expandable Lumbar Interbody Fusion (LIF) Cage System
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K220513 NITRO Interbody Fusion Cage System Family
K220334 MONET Anterior Cervical Plate System
K211785 CASSATT™ SIJ Fixation System
K213491 Universal Pilot Guidance Instrument System
K192863 MONDRIAN Lumbar Interbody Fusion Cage System
K182151 MONET Anterior Cervical Interbody Fusion Cage System with Supplementary Fixation Plate
K172788 MONET™ Anterior Cervical Interbody Fusion Cage System
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