510(k) K243509

Device
Archer PSI System
Applicant
3D-Side
510(k) number
K243509
Product code
QHE
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-12
Date received
2024-11-12
Regulation
888.3660
Classification name
Shoulder Arthroplasty Implantation System
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
Florence Allé
Address
Rue André Dumont 5 Mont-Saint-Guibert BE 1435 1435

FDA Registration Numbers

Source Documents

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

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