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Tornier Perform™ Patient-Matched Primary Reversed Glenoid and BLUEPRINT™ Patient Specific Instrumentation

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211359
510(k) Type
Traditional
Applicant
Tornier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2021
Days to Decision
193 days
Submission Type
Summary

Tornier Perform™ Patient-Matched Primary Reversed Glenoid and BLUEPRINT™ Patient Specific Instrumentation

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211359
510(k) Type
Traditional
Applicant
Tornier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2021
Days to Decision
193 days
Submission Type
Summary