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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)
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)
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