Last synced on 25 January 2026 at 3:41 am

BLUEPRINT™ Patient Specific Instrumentation

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232265
510(k) Type
Traditional
Applicant
Tornier S.A.S.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232265
510(k) Type
Traditional
Applicant
Tornier S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/21/2024
Days to Decision
205 days
Submission Type
Summary