510(k) K250013

Device
VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S, VS8-MP90S, VS8-MP100B, VS10-MP100B, VS11-MP60S, VS11-MP90S, VS12-MP100B, 7F-MP60S, 7F-MP90S, 8F-MP60S, 8F-MP100B, 10F-MP100B, 11F-MP60S, 11F-MP90S, 11P-MP60S, 11P-MP90S, 12F-MP100B, V30-ASP)
Applicant
Control Medical Technology, Inc. / Dba Ventiv Scientific
510(k) number
K250013
Product code
QEZ
Decision
Substantially Equivalent (SESE)
Decision date
2025-03-24
Date received
2025-01-02
Regulation
870.5150
Classification name
Aspiration Thrombectomy Catheter
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Shawn Fojtik
Address
2757 S. 300 W. Suite F Salt Lake City UT US 84115 84115

FDA Registration Numbers

Source Documents

510(k) summary PDF

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