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BLUEPRINT™ Patient Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K232265
510(k) Type
Traditional
Applicant
Tornier SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/21/2024
Days to Decision
205 days
Submission Type
Summary

BLUEPRINT™ Patient Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K232265
510(k) Type
Traditional
Applicant
Tornier SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/21/2024
Days to Decision
205 days
Submission Type
Summary