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Hexanium ACIF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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