MODULAR FOOT SYSTEM

Plate, Fixation, Bone

ORTHOHELIX SURGICAL DESIGNS, INC.

The following data is part of a premarket notification filed by Orthohelix Surgical Designs, Inc. with the FDA for Modular Foot System.

Pre-market Notification Details

Device IDK073624
510k NumberK073624
Device Name:MODULAR FOOT SYSTEM
ClassificationPlate, Fixation, Bone
Applicant ORTHOHELIX SURGICAL DESIGNS, INC. 1815 W. MARKET ST. SUITE 205 Akron,  OH  44313
ContactDerek Lewis
CorrespondentDerek Lewis
ORTHOHELIX SURGICAL DESIGNS, INC. 1815 W. MARKET ST. SUITE 205 Akron,  OH  44313
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-12-26
Decision Date2008-03-20
Summary:summary

NIH GUDID Devices

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