Last synced on 14 November 2025 at 11:06 pm

SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM

Page Type
Cleared 510(K)
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)
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