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T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System

Page Type
Cleared 510(K)
510(k) Number
K200880
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2020
Days to Decision
90 days
Submission Type
Summary

T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System

Page Type
Cleared 510(K)
510(k) Number
K200880
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2020
Days to Decision
90 days
Submission Type
Summary