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Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173535
510(k) Type
Special
Applicant
Titan Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2018
Days to Decision
90 days
Submission Type
Summary

Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173535
510(k) Type
Special
Applicant
Titan Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2018
Days to Decision
90 days
Submission Type
Summary