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Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153250
510(k) Type
Traditional
Applicant
RENOVIS SURGICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2016
Days to Decision
128 days
Submission Type
Summary

Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153250
510(k) Type
Traditional
Applicant
RENOVIS SURGICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2016
Days to Decision
128 days
Submission Type
Summary