Last synced on 25 January 2026 at 3:41 am

Hexanium TLIF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210359
510(k) Type
Special
Applicant
Spinevision, S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/10/2021
Days to Decision
30 days
Submission Type
Summary

Hexanium TLIF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210359
510(k) Type
Special
Applicant
Spinevision, S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/10/2021
Days to Decision
30 days
Submission Type
Summary