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Hexanium® ACIF

Page Type
Cleared 510(K)
510(k) Number
K193000
510(k) Type
Traditional
Applicant
SpineVision SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
10/20/2020
Days to Decision
358 days
Submission Type
Summary

Hexanium® ACIF

Page Type
Cleared 510(K)
510(k) Number
K193000
510(k) Type
Traditional
Applicant
SpineVision SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
10/20/2020
Days to Decision
358 days
Submission Type
Summary