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SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121627
510(k) Type
Abbreviated
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2012
Days to Decision
133 days
Submission Type
Summary

SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121627
510(k) Type
Abbreviated
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2012
Days to Decision
133 days
Submission Type
Summary