510(k) K241259

Device
Amplatz Goose Neck Snare Kit
Applicant
Medtronic, Inc.
510(k) number
K241259
Product code
MMX
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-03
Date received
2024-05-06
Regulation
870.5150
Classification name
Device, Percutaneous Retrieval
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Erin Roquemore
Address
710 Medtronic Pkwy. NE Minneapolis MN US 55432 55432

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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