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3D Printed PEEK Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240250
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2024
Days to Decision
231 days
Submission Type
Summary

3D Printed PEEK Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240250
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2024
Days to Decision
231 days
Submission Type
Summary