Last synced on 14 November 2025 at 11:06 pm

Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS Hyperlordotic Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device, Endoskeleton TT Interbody Fusion Device, Endoskeleton TC Interbody Fusion Device, Endoskeleton TCS Interbody Fusion Device, Endoskeleton TL Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K192018
510(k) Type
Special
Applicant
Titan Spine, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2019
Days to Decision
18 days
Submission Type
Summary

Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS Hyperlordotic Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device, Endoskeleton TT Interbody Fusion Device, Endoskeleton TC Interbody Fusion Device, Endoskeleton TCS Interbody Fusion Device, Endoskeleton TL Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K192018
510(k) Type
Special
Applicant
Titan Spine, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2019
Days to Decision
18 days
Submission Type
Summary