510(k) K212552

Device
Correx Software
Applicant
Vilex, LLC
510(k) number
K212552
Product code
KTT
Decision
Substantially Equivalent (SESE)
Decision date
2021-10-12
Date received
2021-08-13
Regulation
888.3030
Classification name
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Louis Monaco
Address
111 Moffitt St. Mcminnville TN US 37110 37110

FDA Registration Numbers

Source Documents

510(k) summary PDF

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