AEQUALIS REVERSED PROSTHESIS

Shoulder Prosthesis, Reverse Configuration

TORNIER

The following data is part of a premarket notification filed by Tornier with the FDA for Aequalis Reversed Prosthesis.

Pre-market Notification Details

Device IDK061439
510k NumberK061439
Device Name:AEQUALIS REVERSED PROSTHESIS
ClassificationShoulder Prosthesis, Reverse Configuration
Applicant TORNIER 161 RUE LAVOISIER MONTBONNOT Saint-ismier Cedex,  FR 38334
ContactMireille Lemery
CorrespondentMireille Lemery
TORNIER 161 RUE LAVOISIER MONTBONNOT Saint-ismier Cedex,  FR 38334
Product CodePHX  
CFR Regulation Number888.3660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-05-24
Decision Date2006-07-20
Summary:summary

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