Last synced on 25 January 2026 at 3:41 am

VertebraLINK Fusion Platform

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162693
510(k) Type
Traditional
Applicant
Facetlink Dba Linkspine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2017
Days to Decision
183 days
Submission Type
Summary

VertebraLINK Fusion Platform

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162693
510(k) Type
Traditional
Applicant
Facetlink Dba Linkspine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2017
Days to Decision
183 days
Submission Type
Summary