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

Omnia Medical Coupler-A™ Anterior Lumbar Plate System; Omnia Medical Coupler-L™ Lateral Lumbar Plate System

K Number: K230424 · Decision Apr 12, 2023
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
11
Review Days
54

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Basic Information

Device Name
Omnia Medical Coupler-A™ Anterior Lumbar Plate System; Omnia Medical Coupler-L™ Lateral Lumbar Plate System
K Number
K230424
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Omnia Medical, LLC
Date Received
February 17, 2023
Decision Date
April 12, 2023
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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Other Clearances by Omnia Medical, LLC

K Number Device Name
K242431 Omnia Medical PsiF DNA™ System
K240623 Omnia Medical TiBrid™-SA System
K223321 Omnia Medical Coupler-C Anterior Cervical Plate
K212612 Omnia Medical TiBrid-SC
K203207 Omnia Medical TiBrid-SA
K192096 Omnia Medical Trauma Screws
K190363 Omnia Medical TiBrid Cervical Cage, Omnia Medical TiBrid Lateral Cage, Omnia Medical TiBrid ALIF Cage, Omnia Medical TiBrid PLIF Cage, Omnia Medical TiBrid TLIF Cage
K191778 Omnia Medical VBR
K183659 Omnia Medical Rotary PLIF System
K172323 Omnia Medical VBR
Search all 11 clearances from Omnia Medical, LLC →