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Juliet® Ti LL Lumbar Interbody Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241321
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
7/18/2024
Days to Decision
69 days
Submission Type
Summary

Juliet® Ti LL Lumbar Interbody Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241321
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
7/18/2024
Days to Decision
69 days
Submission Type
Summary