reSET-O

K173681 · Pear Therapeutics, Inc. · PWE · Dec 10, 2018 · Neurology

Device Facts

• Record ID: K173681
• Device Name: reSET-O
• Applicant: Pear Therapeutics, Inc.
• Product Code: PWE · Neurology
• Decision Date: Dec 10, 2018
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 882.5801
• Device Class: Class 2
• Attributes: Software as a Medical Device, Therapeutic

Indications for Use

reSET-O™ is intended to increase retention of patients with opioid use disorder (OUD) in outpatient treatment by providing cognitive behavioral therapy, as an adjunct to outpatient treatment that includes transmucosal buprenorphine and contingency management, for patients 18 years or older who are currently under the supervision of a clinician. reSET-O is indicated as a prescription-only digital therapeutic.

Device Story

reSET-O is a 12-week prescription digital therapeutic for Opioid Use Disorder (OUD); delivers cognitive behavioral therapy (CBT) via interactive lessons (text, audio, video, animations, graphics) based on Community Reinforcement Approach (CRA). Used in outpatient settings; patient-facing mobile app and clinician-facing web platform. Patients use app to complete lessons, self-report cravings, triggers, and buprenorphine use. Clinicians access reports to monitor patient status and facilitate communication between visits. Device reinforces buprenorphine adherence; intended to increase treatment retention. Benefits include improved engagement with standard-of-care outpatient programs.

Clinical Evidence

Randomized clinical trial (NCT00929253) of 170 patients with OUD. Patients randomized to 12 weeks of Treatment as Usual (TAU) or TAU plus Therapeutic Educational System (TES). TAU included buprenorphine, urine testing, contingency management, and bi-weekly clinician visits. Primary endpoint: treatment retention (dropout rate). Results: TES group dropout rate 17.6% vs. 31.6% in TAU group (p=0.0224). No significant difference in adverse event rates between groups. Abstinence improvement was not established as clinically significant.

Technological Characteristics

Prescription digital therapeutic; patient-facing mobile application and clinician-facing web/PC platform. Delivers CBT content via text, audio, video, and animations. Operates as an adjunct to standard-of-care outpatient treatment including buprenorphine and contingency management. Software-based; no specific hardware materials or energy sources defined beyond mobile/PC hardware requirements.

Indications for Use

Indicated for patients 18+ with opioid use disorder (OUD) currently in outpatient treatment under clinician supervision, as an adjunct to transmucosal buprenorphine and contingency management.

Regulatory Classification

Identification

A computerized behavioral therapy device for psychiatric disorders is a prescription only device intended to provide a computerized version of condition-specific behavioral therapy as an adjunct to clinician supervised outpatient treatment to patients with psychiatric conditions. The digital therapy is intended to provide patients access to therapy tools used during treatment sessions to improve recognized treatment outcomes.

Special Controls

*Classification.* Class II (special controls). The special controls for this device are:(1) Clinical data must be provided to fulfill the following: (i) Describe a validated model of behavioral therapy for the psychiatric disorder; and (ii) Validate the model of behavioral therapy as implemented by the device. (2) Software must be described in detail in the software requirements specification (SRS) and software design specification (SDS). Software verification, validation, and hazard analysis must be performed. Software documentation must demonstrate that the device effectively implements the behavioral therapy model. (3) The following labeling must be provided: (i) Patient and physician labeling must include instructions for use, including images that demonstrate how to interact with the device. (ii) Patient and physician labeling must list compatible devices. (iii) Patient and physician labeling must include a warning that the device is not intended for use as a standalone therapy. (iv) Patient and physician labeling must include a warning that the device does not represent a substitution for the patient's medication. (v) Physician labeling must include a summary of the clinical testing with the device.

Predicate Devices

• reSET (DEN160018)

Submission Summary (Full Text)

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May 23, 2019

Image /page/0/Picture/1 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & 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.

Pear Therapeutics, Inc. Nandini Murthy Regulatory Consultant to Pear Therapeutics, Inc. 745 Atlantic Ave. Boston, Massachusetts 02111

## Re: K173681

Trade/Device Name: reSET-O Regulation Number: 21 CFR 882.5801 Regulation Name: Computerized behavioral therapy device for psychiatric disorders Regulatory Class: Class II Product Code: PWE Dated: August 21, 2019 Received: August 22, 2018

Dear Nandini Murthy:

This letter corrects our substantially equivalent letter of December 10, 2018.

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

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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 https://www.fda.gov/CombinationProducts/GuidanceRegulatoryInformation/ucm597488.htm); good manufacturing practice requirements as set forth in the quality systems (OS) 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 http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm.

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/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). 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 (http://www.fda.gov/DICE) for more information or contact DICE by email ([e-mail]) or phone [phone] or 301-796-7100).

Sincerely.

Carlos Pena, PhD, MS Director OHT5: Office of Neurological and Physical Medicine Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health

Enclosure

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# Indications for Use

510(k) Number (if known) K173681

Device Name reSET-O

Indications for Use (Describe)

reSET-O™ is intended to increase retention of patients with opioid use disorder (OUD) in outpatient treatment by providing cognitive behavioral therapy, as an adjunct to outpatient that includes transmucosal buprenorphine and contingency management, for patients 18 years or older who are currently under the supervision of a clinician. reSET-O is indicated as a prescription-only digital therapeutic.

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

| <span>☑ Prescription Use (Part 21 CFR 801 Subpart D)</span> |
|-------------------------------------------------------------|
| <span>☐ Over-The-Counter Use (21 CFR 801 Subpart C)</span> |

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#### Appendix 2A. 510 (k) Summary [Clean Version]

#### Pear Therapeutics, Inc.

Traditional 510(k) Premarket Notification Submission - reSET-O

## 510(k) SUMMARY

| Submitter Name: | Pear Therapeutics, Inc. |
|----------------------------|------------------------------------------------------------------|
| Submitter Address: | 201 Mission St., San Francisco, CA 94710 |
| Contact Person: | Yuri Maricich |
| Phone Number: | [phone] |
| Submission Correspondent: | David Amor |
| Phone Number: | [phone] |
| Date Prepared: | November 19, 2018 |
| Device Trade Name: | reSET-O |
| Device Common Name: | Prescription Digital Therapeutic |
| Classification regulation: | 21 CFR 882.5801, Class II Product Code PWE |
| Predicate Device: | reSET, DEN160018 |
| Classification Name: | Computerized Behavioral Therapy Device for Psychiatric Disorders |

## Device Description:

reSET-O™ is a 12-week interval prescription digital therapeutic for Opioid Use Disorder (OUD). reSET-O™ is modeled on the Community Reinforcement Approach (CRA) and engineered to deliver behavioral therapy for patients with OUD. reSET-O™ delivers CRA therapy as a series of interactive therapy lessons. Each therapy lesson is comprised of a cognitive behavioral therapy component and skill building exercises. Therapy lesson content is delivered primarily via text or audio, and may include videos, animations and graphics.

reSET-O™ is intended as an adjunct to standard of care for patients with OUD. It is limited to persons with a valid prescription from their licensed provider. reSET-O™ supports clinician-patient communication between visits, by providing a means for patients to self-report cravings and triggers, and buprenorphine use/non-use. reSET-O™ reinforces the importance of using buprenorphine for treatment of OUD.

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#### Pear Therapeutics, Inc.

Traditional 510(k) Premarket Notification Submission – reSET-O

## Indications for Use:

reSET-O™ is intended to increase retention of patients with opioid use disorder (OUD) in outpatient treatment by providing cognitive behavioral therapy, as an adjunct to outpatient treatment that includes transmucosal buprenorphine and contingency management, for patients 18 years or older who are currently under the supervision of a clinician. reSET-O is indicated as a prescription-only digital therapeutic.

#### Comparison of reSET-O versus predicate Rationale for Substantial Equivalence:

| Characteristics | reSET-O<br>K173681 | reSET (Predicate)<br>DEN160018 |
|---------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Product Code | 21 CFR 882.5801<br>PWE | 21 CFR 882.5801<br>PWE |
| Intended Use | Intended to increase retention in<br>patients with Opioid Use Disorder<br>(OUD) | Intended to increase abstinence<br>and retention in patients with<br>Substance Use Disorder (SUD) |
| Indications for Use | reSET-O™ is intended to<br>increase retention of patients with<br>opioid use disorder (OUD) in<br>outpatient treatment by providing<br>cognitive behavioral therapy, as<br>an adjunct to outpatient treatment<br>with transmucosal buprenorphine<br>and contingency management, for<br>patients 18 years or older who are<br>currently under the supervision of<br>a clinician. reSET-O is indicated<br>as a prescription-only digital<br>therapeutic. | reSET is intended to provide<br>cognitive behavioral therapy, as an<br>adjunct to a contingency<br>management system, for patients 18<br>years of age and older who are<br>currently enrolled in outpatient<br>treatment under the supervision of a<br>clinician. reSET is indicated as a 12<br>week (90 days) prescription-only<br>treatment for patients with<br>substance use disorder (SUD), who<br>are not currently on opioid<br>replacement therapy, who do not<br>abuse alcohol solely, or who do not<br>abuse opioids as their primary<br>substance of abuse. It is intended to:<br>increase abstinence from a<br>●<br>patient's substances of<br>abuse during treatment, and<br>increase retention in the<br>●<br>outpatient treatment<br>program. |

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| Characteristics | reSET-O<br>K173681 | reSET (Predicate)<br>DEN160018 |
|---------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| System<br>components | Patient facing app, mobile device<br>platform<br>Clinician facing app, PC/web<br>platform | Patient facing app, mobile device<br>platform<br>Clinician facing app, PC/web<br>platform |
| Access | Rx only | Rx only |
| Users | Patients with an opioid use<br>disorder. | Patients with a substance use<br>disorder who are not currently on<br>opioid replacement therapy,<br>abuse alcohol solely or whose<br>primary substance of abuse is<br>opioids. |
| Contingency<br>Management | Yes | Yes |
| Adjunctive<br>application | Yes - to Treatment as Usual<br>(TAU), that includes<br>transmucosal buprenorphine in<br>addition to outpatient treatment<br>and contingency management | Yes - to Treatment as Usual<br>(TAU), that includes outpatient<br>treatment and contingency<br>management |

reSET-O™ and reSET® are both prescription devices, with similar application for use in an outpatient treatment program (standard of care). Retention in the program is a key goal in outpatient treatment for any substance use disorder. Both reSET and reSET-O are adjunctive to standard of care. The only difference with the standard of care for patients with OUD (reSET-O™) is that it includes pharmacotherapy (buprenorphine) along with outpatient treatment.

# Performance Data:

Bench data: The results of bench software verification and validation testing supports that reSET-O functions as intended.

Clinical data: reSET-O was validated to meet its intended use in a randomized clinical trial! (Clinical Trials identifier, NCT00929253). The study enrolled 170 patients seeking treatment for OUD. All study participants met DSM-IV criteria for opioid dependence

¹ Christensen DR, Landes RD, Jackson L, et al. Adding an Internet-delivered treatment to an efficacious treatment package for opioid dependence. J Consult Clin Psychol. 2014;82(6):964-972. doi:10.1037/a0037496

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## Pear Therapeutics. Inc.

Traditional 510(k) Premarket Notification Submission - reSET-O

and qualified for buprenorphine treatment. Patients were randomized to 12-weeks of treatment as usual (TAU) or TAU plus (Therapeutic Educational System) TES. TAU included thrice-weekly in-person administration of buprenorphine treatment2, thriceweekly urine testing, contingency management system, and a face to face visit with a clinician every other week. The primary outcome was abstinence defined as the longest documented period of continuous abstinence from opioids and cocaine for each participant.

The results of the clinical study demonstrates that treatment dropout during the 12-week intervention was reduced in the TES group compared to the TAU group. The dropout rate in the TES group was 17.6% compared to 31.6% in the TAU group, with a p-yalue of 0.0224. This reduction in treatment dropout was significant.

Abstinence was evaluated for trend over 12 weeks in the three times a week Urine Drug Screen (UDS). The ability of reSET-O to improve abstinence has not been established as clinically significant.

Adverse events were collected and monitored throughout the study, and showed that there was no difference in AE rates between the TES and TAU groups.

## Conclusion:

reSET-O has similar indications statements as the predicate device. Both devices are used to provide computerized behavioral therapy to patients suffering from substance use disorder. Both devices are adjunctive to standard of care for patients, intended to provide and reinforce therapy delivered in outpatient treatment. Both devices include self-report features that allow the patient and clinician to recognize patterns related to substance use, triggers and cravings.

Preclinical software testing and pivotal clinical study results validate reSET-O towards its proposed intended use. Further, reSET-O met all of the Special controls per the requirements of the predicate (DEN160018).

Therefore, reSET-O is substantially equivalent to the predicate reSET device.

² Buprenorphine treatment consisted of buprenorphine/naloxone combination administered sublingually (4:1) ratio during the 12-week study