510(k) K253376

Device
OBSIDIO™ Conformable Embolic (M0013972101010)
Applicant
Boston Scientific Corporation
510(k) number
K253376
Product code
KRD
Decision
Substantially Equivalent (SESE)
Decision date
2025-10-30
Date received
2025-09-30
Regulation
870.3300
Classification name
Device, Vascular, For Promoting Embolization
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Liz Johnston
Address
One Scimed Pl. Maple Grove MN US 55311 55311

FDA Registration Numbers

Source Documents

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

Other 510(k) Records For Product Code KRD

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K253677Tembo Embolic SystemInstylla, Inc.2025-12-15
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K250133HARBOR Occlusion DeviceNuvascular, Inc.2025-07-09
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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
K240261Siege Vascular Plug (SVP2.5-0.021); Siege Vascular Plug (SVP4-0.021); Siege Vascular Plug (SVP6-0.027)Merit Medical Systems, Inc.2024-05-02