Class Class II

LINQ II Insertable Cardiac Monitor, CareLink SmartSync LINQ II ICM Application (K230553)

K230553 2023-04-26 Traditional
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Description

LINQ II Insertable Cardiac Monitor, CareLink SmartSync LINQ II ICM Application by Medtronic, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230553
Clearance Date2023-04-26
Clearance TypeTraditional
Product CodeMXD
Regulation Number870.1025

Categories

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Predicate lineage for K230553

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. LINQ II Insertable Cardiac Monitor, CareLink SmartSync LINQ II ICM Application (K230553) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K211304LINQ II Insertable Cardiac MonitorMedtronic, Inc.2021

Trace the full predicate network for K230553

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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