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Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241491
510(k) Type
Traditional
Applicant
Stryker Corporation (Tornier, S.A.S.)
Country
France
FDA Decision
Substantially Equivalent
Decision Date
10/10/2024
Days to Decision
139 days
Submission Type
Summary

Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241491
510(k) Type
Traditional
Applicant
Stryker Corporation (Tornier, S.A.S.)
Country
France
FDA Decision
Substantially Equivalent
Decision Date
10/10/2024
Days to Decision
139 days
Submission Type
Summary