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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K223853

Medartis APTUS® Ulna Plates · Medartis AG · decided 2023-03-30 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
APTUSA-4750.98TPMedartis AGHRS07630894801709
APTUSA-6602.117Medartis AGHRS07630894801747
APTUSA-4750.94Medartis AGHRS07630894801600
APTUSA-4750.94TPMedartis AGHRS07630894801686
APTUSA-4750.97SMedartis AGHRS07630894801655
APTUSA-4750.93SMedartis AGHRS07630894801631
APTUSA-4750.93TPMedartis AGHRS07630894801679
APTUSA-4750.98Medartis AGHRS07630894801624
APTUSA-4750.93Medartis AGHRS07630894801594
APTUSA-4750.97TPMedartis AGHRS07630894801693
APTUSA-4750.94SMedartis AGHRS07630894801648
APTUSA-4750.97Medartis AGHRS07630894801617
APTUSA-4750.98SMedartis AGHRS07630894801662
APTUSA-6602.119Medartis AGHRS07630894801754