Last synced on 14 November 2025 at 11:06 pm

BLUEPRINT Patient Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K160555
510(k) Type
Special
Applicant
TORNIER SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/10/2016
Days to Decision
102 days
Submission Type
Summary

BLUEPRINT Patient Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K160555
510(k) Type
Special
Applicant
TORNIER SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/10/2016
Days to Decision
102 days
Submission Type
Summary