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SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K210472
510(k) Type
Special
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/19/2021
Days to Decision
30 days
Submission Type
Summary

SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K210472
510(k) Type
Special
Applicant
Spineart
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/19/2021
Days to Decision
30 days
Submission Type
Summary