Last synced on 14 November 2025 at 11:06 pm

Hexanium ACIF

Page Type
Cleared 510(K)
510(k) Number
K221578
510(k) Type
Special
Applicant
SpineVision, S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/14/2022
Days to Decision
166 days
Submission Type
Summary

Hexanium ACIF

Page Type
Cleared 510(K)
510(k) Number
K221578
510(k) Type
Special
Applicant
SpineVision, S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/14/2022
Days to Decision
166 days
Submission Type
Summary