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Lateral Plate System

Page Type
Cleared 510(K)
510(k) Number
K190016
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2019
Days to Decision
160 days
Submission Type
Summary

Lateral Plate System

Page Type
Cleared 510(K)
510(k) Number
K190016
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2019
Days to Decision
160 days
Submission Type
Summary