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BLUEPRINT Patient Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K162800
510(k) Type
Traditional
Applicant
TORNIER SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/22/2017
Days to Decision
140 days
Submission Type
Summary

BLUEPRINT Patient Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K162800
510(k) Type
Traditional
Applicant
TORNIER SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/22/2017
Days to Decision
140 days
Submission Type
Summary