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Integral Titanium Cervical Interbody

Page Type
Cleared 510(K)
510(k) Number
K222015
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2023
Days to Decision
362 days
Submission Type
Summary

Integral Titanium Cervical Interbody

Page Type
Cleared 510(K)
510(k) Number
K222015
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2023
Days to Decision
362 days
Submission Type
Summary