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T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Tibial Nailing System, T2 Femoral System, T2 Supracondylar Nail System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203819
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2021
Days to Decision
59 days
Submission Type
Summary

T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Tibial Nailing System, T2 Femoral System, T2 Supracondylar Nail System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203819
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2021
Days to Decision
59 days
Submission Type
Summary