LINQ II™ Insertable Cardiac Monitor (ICM)

K240693 · Medtronic, Inc. · MXD · Mar 28, 2024 · Cardiovascular

Device Facts

• Record ID: K240693
• Device Name: LINQ II™ Insertable Cardiac Monitor (ICM)
• Applicant: Medtronic, Inc.
• Product Code: MXD · Cardiovascular
• Decision Date: Mar 28, 2024
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 870.1025
• Device Class: Class 2
• Attributes: Pediatric

Intended Use

The LINQ II ICM is an insertable automatically-activated and patient-activated monitoring system that records subcutaneous ECG and is indicated in adult patients, and in pediatric patients who are at least 2 years old, in the following cases: · patients with clinical syndromes or situations at increased risk of cardiac arrhythmias · patients who experience transient symptoms such as dizziness, palpitation, syncope, and chest pain that may suggest a cardiac arrhythmia

Device Story

LINQ II ICM is an insertable, subcutaneous cardiac monitor; continuously records ECG; automatically detects arrhythmias (tachyarrhythmia, bradyarrhythmia, pause, atrial tachyarrhythmia, atrial fibrillation); supports patient-initiated symptom recording via MyCareLink Heart App or Patient Assistant (Model PA97000). Implanted by physician; small form factor; sapphire/titanium construction. Data transmitted to CareLink Network for clinician review. Enables long-term cardiac rhythm monitoring; assists in diagnosis of transient symptoms; facilitates clinical decision-making regarding arrhythmia management.

Clinical Evidence

Bench testing only. Verification and validation activities were performed to evaluate the modified feedthrough via interface bond strength. Results met all pre-determined acceptance criteria, demonstrating no adverse impact on device function or performance compared to the predicate.

Technological Characteristics

Implantable hermetic enclosure; hybrid sapphire substrate; titanium foil antenna/electrodes; titanium nitride electrode coating; lithium anode/silver vanadium oxide/carbon monofluoride battery (167 mAh). Small form factor. Continuous subcutaneous ECG sensing. Connectivity via telemetry to mobile app/programmer. Software-based arrhythmia detection. Materials: Sapphire, Titanium, Parylene, Titanium Nitride.

Indications for Use

Indicated for adult and pediatric patients (≥2 years) with clinical syndromes/situations at increased risk of cardiac arrhythmias or experiencing transient symptoms (dizziness, palpitation, syncope, chest pain) suggestive of cardiac arrhythmia.

Regulatory Classification

Identification

The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.

Special Controls

*Classification.* Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Arrhythmia Detector and Alarm” will serve as the special control. See § 870.1 for the availability of this guidance document.

Predicate Devices

• LINQ II Insertable Cardiac Monitor (Model LNQ22) (K233320)

Submission Summary (Full Text)

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March 28, 2024

Medtronic, Inc. Andrea Artman Senior Principal Regulatory Affairs Specialist 8200 Coral Sea Street NE Mounds View, Minnesota 55112

Re: K240693

Trade/Device Name: LINQ II Insertable Cardiac Monitor (ICM) Regulation Number: 21 CFR 870.1025 Regulation Name: Arrhythmia Detector And Alarm (Including ST-Segment Measurement And Alarm) Regulatory Class: Class II Product Code: MXD Dated: March 13, 2024 Received: March 13, 2024

Dear Andrea Artman:

We have reviewed your section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (the Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device"

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(https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).

Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30. Design controls; 21 CFR 820.90. Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review. the OS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.

For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email ([e-mail]) or phone [phone] or 301-796-7100).

Sincerely.

Jessica L. Batista -S

tally signed by Jessica : 2024.03.28 18:08:54

for

Sara Royce Assistant Director Division of Cardiac Electrophysiology, Diagnostics and Monitoring Devices

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Office of Cardiovascular Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health

Enclosure

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#### Indications for Use

Submission Number (if known)

K240693

Device Name

LINQ IITM Insertable Cardiac Monitor (ICM)

Indications for Use (Describe)

The LINQ II ICM is an insertable automatically-activated and patient-activated monitoring system that records subcutaneous ECG and is indicated in adult patients, and in pediatric patients who are at least 2 years old, in the following cases:

· patients with clinical syndromes or situations at increased risk of cardiac arrhythmias

· patients who experience transient symptoms such as dizziness, palpitation, syncope, and chest pain that may suggest a cardiac arrhythmia

Type of Use (Select one or both, as applicable)

Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use (21 CFR 801 Subpart C)

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# 510(k) Summary

## Submitter Information

| Date Prepared: | March 12, 2024 |
|--------------------|-------------------------------------------------------------------------------------------------------------------------|
| Submitter: | Medtronic, Inc.<br>Cardiac Rhythm Management<br>8200 Coral Sea Street NE<br>Mounds View, MN 55112<br>ERN: 2182208 |
| Contact Person: | Andrea Artman<br>Sr Prin Regulatory Affairs Specialist<br>Phone: [phone]<br>email: [e-mail] |
| Alternate Contact: | Syed Mohiuddin<br>Regulatory Affairs Director<br>Phone: [phone]<br>email: [e-mail] |

#### General Information

| Trade Name: | LINQ II™ Insertable Cardiac Monitor (ICM) |
|--------------------|-------------------------------------------------------------------------------|
| Common Name: | Insertable Cardiac Monitor |
| Regulation Number: | 21 CFR 870.1025 |
| Product Code: | MXD |
| Classification: | Class II |
| Special Controls: | Class II Special Controls Guidance Document: Arrhythmia Detector and<br>Alarm |
| Predicate Device: | LINQ™ II Insertable Cardiac Monitor (Model LNQ22) K233320 |

## Device Description

The LINQ II Insertable Cardiac Monitor (ICM) Model LNQ22 is a programmable device that continuously monitors a patient's ECG and other physiological parameters. The device records cardiac information in response to automatically detected arrhythmias and patient-initiated activation or markings. The device is designed to automatically record the occurrence of an episode of arrhythmia in a patient. Note: Arrhythmias are classified as tachyarrhythmia, bradyarrhythmia, pause, atrial tachyarrhythmia, or atrial fibrillation. Patients may also manually record symptoms. To manually record symptoms, the patient will also need either the

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MyCareLink Heart App (patient app on mobile device) or the Patient Assistant Model PA97000. The patient can use the MyCareLink Heart App or the Patient to manually record his or her cardiac rhythm while experiencing or immediately after a symptomatic event.

### Accessories

The LINO II ICM includes the following accessories:

- The LINQ Tool Kit Model LNQ22TK includes two implant tools: The Incision Tool is ● used to make a small incision through the patient's skin; and the Insertion Tool is used to insert the device through the incision and into the patient's body at the desired location.
- The Reveal LINQ™ Mobile Manager (LMM) Model MSW002 is the programmer ● designed as a mobile app that communicates with the Reveal LINO and LINO II ICM devices via the existing model 24967 telemetry head.
- . The 2692 Device Command Library (DCL) software is a component of the Data Transformation Services subsystem of the CareLink Network. This software is responsible for understanding command status, implant device state within CareLink, and the initiation of commands for the implanted device.
- The 2691 Instrument Command Library (ICL) software is the logic and data files required ● for remote programming.

## Indications for Use

The LINQ II ICM is an insertable automatically-activated and patient-activated monitoring system that records subcutaneous ECG and is indicated in adult patients, and in pediatric patients who are at least 2 years old, in the following cases:

- . patients with clinical syndromes or situations at increased risk of cardiac arrhythmias
- patients who experience transient symptoms such as dizziness, palpitation, syncope, and ● chest pain that may suggest a cardiac arrhythmia.

# Technological Characteristics

The predicate LINQ II ICM consists of a hybrid substrate that is made of sapphire. The sapphire provides part of the implantable hermetic enclosure. integrates the feedthroughs directly into the substrate, and provides a substrate for component attachment/interconnect. The antenna and sense electrodes are titanium foil laser bonded to the sapphire substrate and connected directly to the embedded feedthroughs. The sense electrodes are coated with sputtered titanium nitride. The sapphire is laser bonded to the titanium battery cover, which provides the complete hermetic enclosure. The battery is Lithium anode, silver vanadium oxide/carbon monofluoride cathode with a capacity of 167 mAh.

The subject LINQ II ICM will continue to use the same technology. It is designed to automatically record the occurrence of an arrhythmia in a patient, continuously sense the patient's subcutaneous ECG, and analyze the timing of ventricular events to detect possible

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episodes of arrhythmia. The LINQ II ICM has a small form factor, and uses Sapphire, Titanium, Parylene, and Titanium Nitride coating on the sensing electrodes as body contacting materials.

When compared to the predicate LINQ II ICM (K233320), the modified LINQ II ICM described herein has the same:

- Intended use/indications for use ●
- Operating principle
- Design features ●
- Device functionality
- Biological safety
- Packaging materials ●
- Shelf life ●

The modified LINQ II ICM differs from the predicate in that the modified device introduces a new design output requiring a minimum bond strength at the feedthrough via interface.

# Substantial Equivalence

Technological differences between the subject and predicate devices have been evaluated with design verification and validation activities. The objective evidence from the evaluation provides assurance of substantial equivalence.

The modified LINQ II ICM is substantially equivalent to the specified predicate device based on comparisons of the device functionality, technological characteristics, and indications for use. The modifications to the subject device were verified and validated through design verification and validation activities. All verification and validation activities were completed successfully and demonstrated there was no adverse impact to the function of the modified LINQ II ICM.

# Conclusion

The results of verification and validation activities met pre-determined acceptance criteria and did not raise new safety or performance issues. Therefore, the modifications made to the LINQ II ICM described herein result in a device that is substantially equivalent to the predicate.