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3D Printed PEEK Interbody System

Page Type
Cleared 510(K)
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)
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