SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM

Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate

SMITH & NEPHEW, INC.

The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Redapt Revision Femoral System.

Pre-market Notification Details

Device IDK121627
510k NumberK121627
Device Name:SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM
ClassificationProsthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate
Applicant SMITH & NEPHEW, INC. 7135 Goodlett Farms Parkway Cordova,  TN  38016
ContactNatalie P Williams
CorrespondentNatalie P Williams
SMITH & NEPHEW, INC. 7135 Goodlett Farms Parkway Cordova,  TN  38016
Product CodeMEH  
CFR Regulation Number888.3353 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeAbbreviated
3rd Party ReviewedNo
Combination ProductNo
Date Received2012-06-04
Decision Date2012-10-15
Summary:summary

NIH GUDID Devices

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