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JOURNEY II XR Knee Instruments

Page Type
Cleared 510(K)
510(k) Number
K173331
510(k) Type
Special
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2017
Days to Decision
24 days
Submission Type
Summary

JOURNEY II XR Knee Instruments

Page Type
Cleared 510(K)
510(k) Number
K173331
510(k) Type
Special
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2017
Days to Decision
24 days
Submission Type
Summary