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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
510(k) Number K212552
Device Name Correx Software
Applicant
Vilex, LLC
111 Moffitt St.
Mcminnville,  TN  37110
Applicant Contact Louis Monaco
Correspondent
Telos Partners, LLC
571 Christina Lake Dr.
Lakeland,  FL  33813
Correspondent Contact Roshana Ahmed
Regulation Number888.3030
Classification Product Code
KTT  
Subsequent Product Code
JDW  
Date Received08/13/2021
Decision Date 10/12/2021
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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