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Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device

Page Type
Cleared 510(K)
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)
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