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Corelink Foundation 3D Anterior Lumbar System

Page Type
Cleared 510(K)
510(k) Number
K180556
510(k) Type
Special
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2018
Days to Decision
148 days
Submission Type
Summary

Corelink Foundation 3D Anterior Lumbar System

Page Type
Cleared 510(K)
510(k) Number
K180556
510(k) Type
Special
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2018
Days to Decision
148 days
Submission Type
Summary