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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230424
510(k) Type
Traditional
Applicant
Omnia Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2023
Days to Decision
54 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230424
510(k) Type
Traditional
Applicant
Omnia Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2023
Days to Decision
54 days
Submission Type
Summary