510(k) K253551

Device
VELYS™ Hip Navigation
Applicant
Depuy Ireland UC
510(k) number
K253551
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-06
Date received
2025-11-14
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Erin Combs
Address
Loughbeg Ringaskiddy, Co. Cork IE

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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