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CoreLink® M3™ Stand-Alone Anterior Lumbar System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180814
510(k) Type
Traditional
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2018
Days to Decision
134 days
Submission Type
Summary

CoreLink® M3™ Stand-Alone Anterior Lumbar System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180814
510(k) Type
Traditional
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2018
Days to Decision
134 days
Submission Type
Summary