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Nanovis Intervertebral Body Fusion System and FortiCore®

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160874
510(k) Type
Special
Applicant
Nanovis, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2016
Days to Decision
90 days
Submission Type
Summary

Nanovis Intervertebral Body Fusion System and FortiCore®

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160874
510(k) Type
Special
Applicant
Nanovis, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2016
Days to Decision
90 days
Submission Type
Summary