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REDAPT Porous Acetabular Shell

Page Type
Cleared 510(K)
510(k) Number
K181366
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2018
Days to Decision
124 days
Submission Type
Summary

REDAPT Porous Acetabular Shell

Page Type
Cleared 510(K)
510(k) Number
K181366
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2018
Days to Decision
124 days
Submission Type
Summary