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CoreLink Midline Fixation System

Page Type
Cleared 510(K)
510(k) Number
K210539
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2021
Days to Decision
50 days
Submission Type
Summary

CoreLink Midline Fixation System

Page Type
Cleared 510(K)
510(k) Number
K210539
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2021
Days to Decision
50 days
Submission Type
Summary