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Endoskeleton TCS Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K151596
510(k) Type
Traditional
Applicant
TITAN SPINE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2015
Days to Decision
119 days
Submission Type
Summary

Endoskeleton TCS Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K151596
510(k) Type
Traditional
Applicant
TITAN SPINE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2015
Days to Decision
119 days
Submission Type
Summary