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SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
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)
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