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Endoskeleton TL Interbody Fusion Device, Endoskeleton TL 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
K191581
510(k) Type
Traditional
Applicant
Titan Spine, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2020
Days to Decision
208 days
Submission Type
Summary

Endoskeleton TL Interbody Fusion Device, Endoskeleton TL 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
K191581
510(k) Type
Traditional
Applicant
Titan Spine, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2020
Days to Decision
208 days
Submission Type
Summary