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Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163269
510(k) Type
Traditional
Applicant
TITAN SPINE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2017
Days to Decision
143 days
Submission Type
Summary

Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163269
510(k) Type
Traditional
Applicant
TITAN SPINE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2017
Days to Decision
143 days
Submission Type
Summary