Last synced on 16 May 2025 at 11:05 pm

SpineJack Expansion Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181262
510(k) Type
Traditional
Applicant
Vexim SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/30/2018
Days to Decision
111 days
Submission Type
Summary

SpineJack Expansion Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181262
510(k) Type
Traditional
Applicant
Vexim SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/30/2018
Days to Decision
111 days
Submission Type
Summary