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F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and Oro Lateral Plate System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231743
510(k) Type
Traditional
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2023
Days to Decision
177 days
Submission Type
Summary

F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and Oro Lateral Plate System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231743
510(k) Type
Traditional
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2023
Days to Decision
177 days
Submission Type
Summary