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Genesis II XLPE Resurfacing Patellar Components

Page Type
Cleared 510(K)
510(k) Number
K150241
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2015
Days to Decision
267 days
Submission Type
Summary

Genesis II XLPE Resurfacing Patellar Components

Page Type
Cleared 510(K)
510(k) Number
K150241
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2015
Days to Decision
267 days
Submission Type
Summary