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VertebraLINK Fusion Platform

Page Type
Cleared 510(K)
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)
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