Last synced on 25 April 2025 at 11:05 pm

ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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