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Endoskeleton TO Interbody Fusion Device (IBD)

Page Type
Cleared 510(K)
510(k) Number
K170399
510(k) Type
Traditional
Applicant
Titan Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2017
Days to Decision
147 days
Submission Type
Summary

Endoskeleton TO Interbody Fusion Device (IBD)

Page Type
Cleared 510(K)
510(k) Number
K170399
510(k) Type
Traditional
Applicant
Titan Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2017
Days to Decision
147 days
Submission Type
Summary