510(k) K240261

Device
Siege Vascular Plug (SVP2.5-0.021); Siege Vascular Plug (SVP4-0.021); Siege Vascular Plug (SVP6-0.027)
Applicant
Merit Medical Systems, Inc.
510(k) number
K240261
Product code
KRD
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-02
Date received
2024-01-31
Regulation
870.3300
Classification name
Device, Vascular, For Promoting Embolization
Medical specialty
Cardiovascular
Review panel
Cardiovascular
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
James Kenny
Address
1600 Merit Pkwy. Bldg. 87 South Jordan UT US 84095 84095

FDA Registration Numbers

Source Documents

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

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K250079Ruby XL SystemPenumbra, Inc.2025-03-14
K242608Embozene Color-Advanced MicrospheresVarian Medical Systems, Inc.2025-01-17
K240873TEMBO Embolic SystemInstylla, Inc.2024-12-16
K242794ONCOZENE MicrospheresVarian Medical Systems, Inc.2024-10-16
K242507OBSIDIO™ Conformable EmbolicBoston Scientific2024-10-03
K232934SunsphereHangzhou Yangshun Medical Technology Co.,Ltd2024-05-30