510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K233320Substantially Equivalent

LINQ II™ Insertable Cardiac Monitor (LNQ22)

Medtronic, Inc., Mounds View MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K233320 is the FDA 510(k) clearance record for LINQ II™ Insertable Cardiac Monitor (LNQ22), a class II device, cleared for Medtronic, Inc. on under FDA product code MXD (Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show one recall naming K233320.

Clearance record

Decision date
Received
(32 days to decision)
Product code
MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
Regulation
21 CFR 870.1025
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronic, Inc. Cardiovascular Diagnostics And Services, Mounds View MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MXD

Trailing 12 months
3 clearances under product code MXD in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MXD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20261
September 20260
October 20260