TRIGEN HINDFOOT FUSION NAIL

Rod, Fixation, Intramedullary And Accessories

SMITH & NEPHEW, INC.

The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Trigen Hindfoot Fusion Nail.

Pre-market Notification Details

Device IDK043052
510k NumberK043052
Device Name:TRIGEN HINDFOOT FUSION NAIL
ClassificationRod, Fixation, Intramedullary And Accessories
Applicant SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis,  TN  38116
ContactJanet Johnson Akil
CorrespondentJanet Johnson Akil
SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis,  TN  38116
Product CodeHSB  
CFR Regulation Number888.3020 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2004-11-05
Decision Date2004-11-24
Summary:summary

NIH GUDID Devices

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