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Smith & Nephew, Inc. REDAPT Augments

Page Type
Cleared 510(K)
510(k) Number
K171073
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2017
Days to Decision
224 days
Submission Type
Summary

Smith & Nephew, Inc. REDAPT Augments

Page Type
Cleared 510(K)
510(k) Number
K171073
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2017
Days to Decision
224 days
Submission Type
Summary