510(k) K234062

Device
APTUS Hand Scaphoid Plates
Applicant
Medartis AG
510(k) number
K234062
Product code
HRS
Decision
Substantially Equivalent (SESE)
Decision date
2024-03-21
Date received
2023-12-22
Regulation
888.3030
Classification name
Plate, Fixation, Bone
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
Claudia De Santis
Address
Hochbergerstrasse 60e Basel CH 4057 4057

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
07630037812197APTUSMedartis AG2024-10-30
07630894811739APTUSMedartis AG2024-07-26
07630894811722APTUSMedartis AG2024-07-26
07630894811715APTUSMedartis AG2024-07-26
07630894811708APTUSMedartis AG2024-07-26
07630894811692APTUSMedartis AG2024-07-26
07630894811661APTUSMedartis AG2024-07-26
07630894811630APTUSMedartis AG2024-07-26
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07630894811647APTUSMedartis AG2024-07-06
07630894811623APTUSMedartis AG2024-07-06
07630894811616APTUSMedartis AG2024-07-06

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