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QUANTUM Patient Specific Instrumentation (PSI) System

Page Type
Cleared 510(K)
510(k) Number
K230313
510(k) Type
Traditional
Applicant
In2Bones SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/6/2023
Days to Decision
59 days
Submission Type
Summary

QUANTUM Patient Specific Instrumentation (PSI) System

Page Type
Cleared 510(K)
510(k) Number
K230313
510(k) Type
Traditional
Applicant
In2Bones SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/6/2023
Days to Decision
59 days
Submission Type
Summary