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OPTIX H2 Patient Specific Instrument System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230462
510(k) Type
Traditional
Applicant
Vilex, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2023
Days to Decision
146 days
Submission Type
Summary

OPTIX H2 Patient Specific Instrument System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230462
510(k) Type
Traditional
Applicant
Vilex, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2023
Days to Decision
146 days
Submission Type
Summary