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VersaLink™ Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182598
510(k) Type
Traditional
Applicant
Premia Spine, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2018
Days to Decision
54 days
Submission Type
Summary

VersaLink™ Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182598
510(k) Type
Traditional
Applicant
Premia Spine, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2018
Days to Decision
54 days
Submission Type
Summary