Last synced on 14 November 2025 at 11:06 pm

SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K242890
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/7/2025
Days to Decision
165 days
Submission Type
Summary

SPINEART Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K242890
510(k) Type
Traditional
Applicant
Spineart SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/7/2025
Days to Decision
165 days
Submission Type
Summary