510(k) K202730

Device
Quadra-P
Applicant
Medacta International S.A.
510(k) number
K202730
Product code
LZO
Decision
Substantially Equivalent (SESE)
Decision date
2020-12-28
Date received
2020-09-18
Regulation
888.3353
Classification name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Stefano Baj
Address
Strada Regina Castel San Pietro (Ch) CH CH-6874 CH-6874

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
07630971243408Quadra P femoral stemsMedacta International SA2021-01-04

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K243029Origin™ TT StemSignature Orthopaedics Pty, Ltd.2025-03-11
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