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MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK™

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172212
510(k) Type
Traditional
Applicant
CTL Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2018
Days to Decision
169 days
Submission Type
Summary

MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK™

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172212
510(k) Type
Traditional
Applicant
CTL Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2018
Days to Decision
169 days
Submission Type
Summary