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SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K183630
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
6/10/2019
Days to Decision
166 days
Submission Type
Summary

SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K183630
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
6/10/2019
Days to Decision
166 days
Submission Type
Summary