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SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241644
510(k) Type
Special
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
8/7/2024
Days to Decision
61 days
Submission Type
Summary

SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241644
510(k) Type
Special
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
8/7/2024
Days to Decision
61 days
Submission Type
Summary