Last synced on 23 May 2025 at 11:06 pm

NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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