BrainInsight

K220815 · Hyperfine, Inc. · QIH · Jul 19, 2022 · Radiology

Device Facts

• Record ID: K220815
• Device Name: BrainInsight
• Applicant: Hyperfine, Inc.
• Product Code: QIH · Radiology
• Decision Date: Jul 19, 2022
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.2050
• Device Class: Class 2
• Attributes: AI/ML, Software as a Medical Device

Intended Use

BrainInsight is intended for automatic labeling, spatial measurement, and volumetric quantification of brain structures from a set of low-field MR images and returns annotated and segmented images, color overlays and reports.

Device Story

BrainInsight is an automated MR imaging post-processing software; processes low-field MR images (T1/T2 sequences) from Hyperfine Swoop MRI scanners. Uses machine learning-based internal pipeline to perform image alignment, whole brain/ventricle segmentation, and midline shift measurements. Operates in a serverless cloud environment; receives DICOM inputs; returns annotated images, color overlays, and morphometric reports to PACS/DICOM workstations. Used in clinical settings; results reviewed by trained physicians. Benefits include automated, rapid (approx. 7 minutes) quantification of brain structures to assist clinical decision-making regarding brain pathology (e.g., stroke, hemorrhage, tumor, hydrocephalus).

Clinical Evidence

Bench testing only. Performance validated using multi-site datasets (T1/T2 sequences) from Hyperfine Swoop MRI. Ground truth established via expert consensus and STAPLE. Metrics: Midline shift mean absolute error (0.97-1.03 mm); Dice overlap for ventricles (79-84%) and whole brain (95-96%); volume differences (3-19%). Results demonstrate model performance is non-inferior to average human annotator discrepancy.

Technological Characteristics

Automated MR post-processing software; serverless cloud deployment; supports Linux. Uses machine learning-based segmentation and quantification pipeline. Inputs/outputs via DICOM. Automated quality control includes tissue contrast check, scan protocol verification, and atlas alignment check. Software developed per IEC 62304:2006.

Indications for Use

Indicated for automatic labeling, spatial measurement, and volumetric quantification of brain structures from low-field MR images in adults (≥ 18 years).

Regulatory Classification

Identification

A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.

Special Controls

*Classification.* Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).

Predicate Devices

• BrainInsight (K202414)

Submission Summary (Full Text)

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Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health and Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.

Hyperfine, Inc. % Christine Kupchick Sr. Regulatory Specialist 351 New Whitfield Street GUILFORD CT 06437

Re: K220815

July 19, 2022

Trade/Device Name: BrainInsight Regulation Number: 21 CFR 892.2050 Regulation Name: Medical image management and processing system Regulatory Class: Class II Product Code: QIH Dated: June 22, 2022 Received: June 23, 2022

Dear Christine Kupchick:

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 (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 located 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.

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 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see

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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 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 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 medical devices and radiation-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 Lamb, Ph.D. Assistant Director Imaging Software Team DHT8B: Division of Radiological Imaging Devices and Electronic Products OHT8: Office of Radiological Health Office of Product Evaluation and Ouality Center for Devices and Radiological Health

Enclosure

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## Indications for Use

510(k) Number (if known) K220815

Device Name BrainInsight

Indications for Use (Describe)

BrainInsight is intended for automatic labeling, spatial measurement, and volumetric quantification of brain structures from a set of low-field MR images and returns annotated and segmented images, color overlans and reports.

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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# HYPERFINE

# 510(k) SUMMARY K220815

#### 510(k) Submitter

| Company Name: | Hyperfine, Inc. |
|------------------|--------------------------------------------|
| Company Address: | 351 New Whitfield St<br>Guilford, CT 06437 |

#### Contact

| Name: | Christine Kupchick |
|------------|------------------------|
| Telephone: | [phone] |
| Email: | [e-mail] |

July 14, 2022 Date Prepared:

#### Device Identification

| Trade Name: | BrainInsight |
|--------------------|-------------------------------------|
| Common Name: | MR Imaging Post-Processing Software |
| Regulation Number: | 21 CFR 892.2050 |
| Product Code: | QIH |
| Regulatory Class: | Class II |

#### Predicate Device Information

The subject BrainInsight is substantially equivalent to the predicate BrainInsight (K202414). The predicate device has not been subject to a design-related recall.

#### Device Description

BrainInsight is a fully automated MR imaging post-processing medical software that provides image alignment, whole brain segmentation, ventricle segmentation, and midline shift measurements of brain structures from a set of MR images from patients ages 18 years or older. The BrainInsight processing architecture includes a proprietary automated internal pipeline based on machine learning tools. The output annotated and segmented images are provided in standard image format using segmented color overlays and reports that can be displayed on third-party workstations and FDA-cleared Picture Archive and Communications Systems (PACS).

The modified BrainInsight described in this submission includes changes to the machine learning models to allow for the processing Al-reconstructed low-field MR images. The modified device also includes configuration updates and refactoring changes for incremental improvement.

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#### Indications for Use

BrainInsight is intended for automatic labeling, spatial measurement, and volumetric quantification of brain structures from a set of low-field MR images and returns annotated and segmented images, color overlays and reports.

#### Technological Characteristics

The subject device has the same intended use, fundamental technology, and operating principles, as the predicate (K202414). Therefore, the subject device is substantially equivalent to the predicate.

#### Substantial Equivalence Discussion

The table below compares the subject device to the predicate.

| Attribute | Subject BrainInsight | Predicate BrainInsight (K202414) |
|-------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Indications for Use | BrainInsight is intended for automatic labeling,<br>spatial measurement, and volumetric<br>quantification of brain structures from a set of<br>low-field MR images and returns annotated and<br>segmented images, color overlays and reports. | Same |
| Target Anatomical<br>Sites | Brain | Same |
| Patient Population | Adult (≥ 18 years) | Same |
| Technology | Automated measurement of brain tissue<br>volumes and structures of Al-reconstructed<br>low-field MR images Automatic segmentation and quantification<br>of brain structures of Al-reconstructed low-<br>field MR images using machine learning<br>tools | Automated measurement of brain<br>tissue volumes and structures of<br>conventional low-field MR images Automatic segmentation and<br>quantification of brain structures of<br>conventional low-field MR images<br>using machine learning tools |
| Method of Use | MR images are automatically sent to<br>BrainInsight, and processed images are<br>automatically returned in ~7 minutes | Same |
| User Interface /<br>Physical<br>Characteristics | No software required Operates in a serverless cloud environment User interface through PACS (multiple<br>vendors) | Same |
| Operating System | Supports Linux | Same |
| Processing<br>Architecture | Automated internal pipeline that performs:<br>segmentation volume calculation distance measurement numerical information display | Same |
| Data Source | MRI Scanner: Hyperfine Swoop FSE MRI<br>scans acquired with specified protocols Supports DICOM format as input | Same |
| Output | Provides volumetric measurements of brain<br>structures:<br>Includes segmented color overlays and<br>morphometric reports | Same |

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| | Supports DICOM format as output of results that can be displayed on DICOM workstations and PACS | |
|--------|----------------------------------------------------------------------------------------------------------------------------------------------------------------|------|
| Safety | Automated quality control functions:<br>Tissue contrast check Scan protocol verification Atlas alignment check Results must be reviewed by a trained physician | Same |

#### Performance

As part of demonstrating substantial equivalence to the predicate, a risk analysis was completed to identify the risks associated with the software modifications. Software verification as related to the modifications was performed per IEC 62304:2006 and as recommended in the FDA Guidance, "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices." The subject device passed all the testing in accordance with internal requirements and applicable standards to support substantial equivalence.

Each model was trained using a training dataset to optimize parameters and a separate validation dataset to select the best set of parameters. Comparing the training and validation metrics helps to monitor and prevent overfitting. The datasets were augmented to improve robustness using standard techniques that apply transformations to the input data. The testing dataset was separate from training and validation datasets. Each subject was assigned a unique identifier and all subjects in training and validation data were excluded from the test set.

The data collection for the training and validation datasets were done at multiple sites. Each site used the T1 and T2 sequences from the FDA cleared Hyperfine Swoop Portable MR imaging system. The datasets were annotated by multiple experts. The entire group of training image sets was divided into segments and each segment was given to a single expert. The expert's determination became the ground truth for each image set in their segment. Each model and application were validated using an appropriate sample size to yield statistically significant results. All test images were acquired using the latest Swoop software version. The test set had the following distribution:

| Category | Data Distribution |
|-----------|----------------------------------------------------------------------------------------------------|
| Age | Min: 19 Max: 77 |
| Gender | 59% F / 41% M |
| Pathology | Stroke (Infarct) Hydrocephalus Hemorrhage (SAH, SDH, IVH, IPH) Mass/Edema Tumor Multiple sclerosis |

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Quantitative evaluation was performed to validate performance using software. The performance of the model and the annotators to the consensus-based annotation was computed to ensure that the model performance is no worse than the average annotator. The acceptance criteria were defined based on non-inferiority testing, in which the model discrepancy to the annotators can be no worse than the average annotator discrepancy.

The mean absolute error was used to calculate the error range for midline shift. Ground truth for midline shift was determined based on the average shift distance of all annotators.

| Application | T1 Error | T2 Error |
|---------------|----------|----------|
| Midline Shift | 1.03 mm | 0.97 mm |

The mean Dice coefficient was used to calculate the error range for the lateral ventricles and whole brain. Ground truth for segmentation is calculated using Simultaneous Truth and Performance Level Estimation (STAPLE).

| Application | Dice Overlap [%] | | Volume Differences [%] | |
|-----------------|------------------|-----------|------------------------|-----------|
| T1 | Device | Annotator | Device | Annotator |
| Left Ventricle | 84 | 90 | 8 | 8 |
| Right Ventricle | 82 | 89 | 7 | 11 |
| Whole Brain | 95 | 97 | 3 | 2 |

| Application | Dice Overlap [%] | | Volume Differences [%] | |
|-----------------|------------------|-----------|------------------------|-----------|
| T2 | Device | Annotator | Device | Annotator |
| Left Ventricle | 81 | 84 | 11 | 27 |
| Right Ventricle | 79 | 84 | 19 | 26 |
| Whole Brain | 96 | 97 | 5 | 5 |

The test results show high accuracy of BrainInsight performance as compared to the reference and annotators and the subject device met all acceptance criteria.

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#### Conclusion

Based on the indications for use, technological characteristics, performance results, and comparison to the predicate, the subject BrainInsight has been shown to be substantially equivalent to the predicate and does not present any new issues of safety or effectiveness.