Last synced on 25 April 2025 at 11:05 pm

Ti-Diagon Oblique TLIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172064
510(k) Type
Traditional
Applicant
Camber Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2017
Days to Decision
70 days
Submission Type
Summary

Ti-Diagon Oblique TLIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172064
510(k) Type
Traditional
Applicant
Camber Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2017
Days to Decision
70 days
Submission Type
Summary