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Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182007
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2018
Days to Decision
133 days
Submission Type
Summary

Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182007
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2018
Days to Decision
133 days
Submission Type
Summary