TREU; BONE SCREWS, SCHANZ SCREWS, KIRSCHNER WIRES, STEINMANN PINS, LARSEN PINS

Screw, Fixation, Bone

TREU-INSTRUMENTE GMBH

The following data is part of a premarket notification filed by Treu-instrumente Gmbh with the FDA for Treu; Bone Screws, Schanz Screws, Kirschner Wires, Steinmann Pins, Larsen Pins.

Pre-market Notification Details

Device IDK083912
510k NumberK083912
Device Name:TREU; BONE SCREWS, SCHANZ SCREWS, KIRSCHNER WIRES, STEINMANN PINS, LARSEN PINS
ClassificationScrew, Fixation, Bone
Applicant TREU-INSTRUMENTE GMBH GRIESWEG 47 Muhlheim, Baden-wurttemberg,  DE 78570
ContactFranz Menean
CorrespondentFranz Menean
TREU-INSTRUMENTE GMBH GRIESWEG 47 Muhlheim, Baden-wurttemberg,  DE 78570
Product CodeHWC  
Subsequent Product CodeHTY
Subsequent Product CodeJDW
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2008-12-30
Decision Date2009-07-15
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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04048447018437 K083912 000

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