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Hexanium PLIF

Page Type
Cleared 510(K)
510(k) Number
K223251
510(k) Type
Traditional
Applicant
SpineVision, S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
56 days
Submission Type
Summary

Hexanium PLIF

Page Type
Cleared 510(K)
510(k) Number
K223251
510(k) Type
Traditional
Applicant
SpineVision, S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
56 days
Submission Type
Summary