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ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

Page Type
Cleared 510(K)
510(k) Number
K083714
510(k) Type
Traditional
Applicant
TITAN SPINE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2009
Days to Decision
121 days
Submission Type
Summary

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

Page Type
Cleared 510(K)
510(k) Number
K083714
510(k) Type
Traditional
Applicant
TITAN SPINE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2009
Days to Decision
121 days
Submission Type
Summary