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Porous Patella and Porous Tibia Baseplate

Page Type
Cleared 510(K)
510(k) Number
K211221
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2021
Days to Decision
161 days
Submission Type
Summary

Porous Patella and Porous Tibia Baseplate

Page Type
Cleared 510(K)
510(k) Number
K211221
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2021
Days to Decision
161 days
Submission Type
Summary