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NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110442
510(k) Type
Traditional
Applicant
Nanovis, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2011
Days to Decision
266 days
Submission Type
Summary

NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110442
510(k) Type
Traditional
Applicant
Nanovis, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2011
Days to Decision
266 days
Submission Type
Summary