Who is the manufacturer of EARP Nerve Cuff Electrode?

Nvision Biomedical Technologies, Inc. filed the 510(k) submission for EARP Nerve Cuff Electrode (K230853).

What is the FDA product code for EARP Nerve Cuff Electrode?

ETN. It is classified under 21 CFR 874.1820 as a Class 2 device in the Ear, Nose, Throat panel.

What is the regulatory pathway for EARP Nerve Cuff Electrode?

510(k) clearance (submission type: Traditional).

What are the predicate devices for EARP Nerve Cuff Electrode?

Cadwell Lab Disposable Stimulator Probes (K103128); Ad-Tech Medical Cueva Cranial Nerve Electrode (K944061).

Who can help prepare an FDA 510(k) submission like EARP Nerve Cuff Electrode?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

EARP Nerve Cuff Electrode

K230853 · Nvision Biomedical Technologies, Inc. · ETN · Oct 6, 2023 · Ear, Nose, Throat

Device Facts

Record ID	K230853
Device Name	EARP Nerve Cuff Electrode
Applicant	Nvision Biomedical Technologies, Inc.
Product Code	ETN · Ear, Nose, Throat
Decision Date	Oct 6, 2023
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 874.1820
Device Class	Class 2

Intended Use

The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Device Story

EARP Nerve Cuff Electrode is a sterile, single-use surgical accessory for intraoperative neuromonitoring. It functions as a passive conduit for electrical signals between external, commercially available neuromonitoring systems and target neural tissue. The device features a distal C-shaped cuff with platinum contacts for direct nerve engagement and proximal 1.5mm safety socket connectors for equipment interface. During surgery, a clinician (e.g., surgeon or neurophysiologist) positions the cuff around spinal nerve roots to facilitate localized stimulation or monitoring. The device does not generate or record signals independently; it relies on the host neuromonitoring system. By enabling precise nerve identification and monitoring, the device assists the surgeon in avoiding nerve damage, potentially improving surgical outcomes. It is intended for use in an operating room environment.

Clinical Evidence

Bench testing only. No clinical data provided. Testing included dimensional analysis, tensile/flexural testing, electrical safety (high potential/leakage), and biocompatibility (cytotoxicity, sensitization, irritation, acute systemic toxicity, and material-mediated pyrogenicity). All tests passed.

Technological Characteristics

Bipolar nerve cuff electrode. Materials: Platinum contacts, polyimide insulation, silicone cuff, stainless steel lead wire, FEP lead insulation. Dimensions: 2mm strip contact, 1.8m lead length, 260mm applicator. Connectivity: 1.5mm safety socket for external neuromonitoring systems. Sterilization: Sterile, single-use. Standards: ISO 14708-1 (electrical safety), IEC 60601-1 (lead wire performance), ISO 10993 (biocompatibility).

Indications for Use

Indicated for use in patients undergoing surgery requiring localized stimulation, identification, and monitoring of spinal nerve roots.

Regulatory Classification

Identification

A surgical nerve stimulator/locator is a device that is intended to provide electrical stimulation to the body to locate and identify nerves and to test their excitability.

Predicate Devices

Cadwell Lab Disposable Stimulator Probes (K103128)
Ad-Tech Medical Cueva Cranial Nerve Electrode (K944061)

Related Devices

K241917 — EARP Nerve Cuff Electrode · Retropsoas Technologies, LLC · Jul 31, 2024
K111597 — DISPOSABLE STIMULATING ELECTRODE · Nuvasive, Inc. · Oct 13, 2011
K973454 — AD-TECH'S SPINAL ELECTRODE · Ad-Tech Medical Instrument Corp · Jun 10, 1998
K112435 — RHYTHMLINK MONOPOLAR STIMULATING INSTRUMENT · Rhythmlink International, LLC · Sep 22, 2011
K100912 — DISPOSABLE NERVE STIMULATING PROBE, BIPOLAR CONCENTRIC, DISPOSABLE NERVE STIMULATOR PROBE, BIPOLAR SIDE BY SIDE · Kirwan Surgical Products, Inc. · Aug 19, 2010

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the date October 6, 2023. The text is written in a clear, sans-serif font. The date is likely part of a document or calendar entry. The text is horizontally aligned and centered. Image /page/0/Picture/1 description: The image contains 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. Nvision Biomedical Technologies, Inc. % Jeffrey Brittan Vice President of Product Realization Watershed Idea Foundry 1815 Aston Ave.. Suite 106 Carlsbad, California 92008 Re: K230853 Trade/Device Name: EARP Nerve Cuff Electrode Regulation Number: 21 CFR 874.1820 Regulation Name: Surgical Nerve Stimulator/Locator Regulatory Class: Class II Product Code: ETN Dated: September 6, 2023 Received: September 7, 2023 Dear Jeffrey Brittan: 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" {1}------------------------------------------------ (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 (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely. # Patrick Antkowiak -S for Jay Gupta Assistant Director DHT5A: Division of Neurosurgical, Neurointerventional {2}------------------------------------------------ Enclosure {3}------------------------------------------------ ## Indications for Use 510(k) Number (if known) Device Name EARP Nerve Cuff Electrode #### Indications for Use (Describe) The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery. | Type of Use (Select one or both, as applicable) | | |---------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------| | <div> ☑ Prescription Use (Part 21 CFR 801 Subpart D) </div> | <div> ☐ Over-The-Counter Use (21 CFR 801 Subpart C) </div> | #### CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {4}------------------------------------------------ ## 510(k) Summary DATE PREPARED October 4, 2023 ## MANUFACTURER Nvision Biomedical Technologies, Inc. 4590 Lockhill Selma San Antonio, TX 78249, USA Telephone: (210) 545-3713 Fax: (866) 764-1139 Official Contact: Diana Langham, Director of Regulatory and Corporate Compliance #### REPRESENTATIVE/CONSULTANT Jeffrey Brittan Vice President of Product Realization Watershed Idea Foundry Telephone: (714) 287-6780 Email: jeffbrittan(a)watershedideas.com ### PROPRIETARY NAME OF SUBJECT DEVICE EARP Nerve Cuff Electrode COMMON NAME Nerve Stimulator #### DEVICE CLASSIFICATION Surgical nerve stimulator/locator (Classification Regulations: 21 CFR 874.1820, Product Codes: ETN, Class: II) PREMARKET REVIEW Ear, Nose, & Throat #### INDICATIONS FOR USE The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery. #### DEVICE DESCRIPTION The EARP Nerve Cuff Electrode conducts electrical signal as a component of intraoperative neuromonitoring. The EARP Nerve Cuff Electrode is used with commercially available neuromonitoring systems and does not stimulate or record signal itself. The standard connectors at the proximal end of the EARP Nerve Cuff Electrode interface with the neuromonitoring equipment and the distal cuff contacts the target tissue. The EARP Nerve Cuff Electrode is provided sterile packaged and is for single use only. {5}------------------------------------------------ K230853 Page 2 of 3 #### PREDICATE DEVICE IDENTIFICATION The subject EARP Nerve Cuff Electrode is substantially equivalent to the following predicates: | 510(k) Number | Manufacturer & Predicate Device Name | Predicate | |---------------|-----------------------------------------------|------------| | K103128 | Cadwell Lab Disposable Stimulator Probes | Primary | | K944061 | Ad-Tech Medical Cueva Cranial Nerve Electrode | Additional | #### SUMMARY OF NON-CLINICAL TESTING No FDA performance standards have been established for nerve stimulators or electrodes. The EARP Nerve Cuff Electrode was evaluated to ensure that it performed as intended and supported substantial equivalence to the predicate devices. Testing and analysis included: - Analysis of dimensional characteristics, materials, function, and intended use . - Tensile and flexural testing (to verify mechanical integrity, continuity, isolation, and . visual appearance) - Electrical safety testing (high potential and electrical leakage per ISO 14708-1) - Electrode lead wire performance per 21 CFR 898.12 (IEC 60601-1) - Biocompatibility testing including cytotoxicity, sensitization, irritation/intracutaneous . reactivity, acute systemic toxicity, and material-mediated pyrogenicity: | Endpoint | Test Description | Conclusion | Pass/Fail | |------------------------------------------------------------------|-------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------| | Cytotoxicity (ISO 10993-5) | Elution Method (1X MEM extraction vehicle) | The test article extract showed no evidence of causing cell lysis or toxicity. The test article extract met the requirements of the test since the grade was less than a grade 2 (mild reactivity). | Pass | | Sensitization (ISO 10993-10) | Maximization Sensitization Study (Polar and non-polar extraction vehicles) | The test article extracts showed no evidence of causing delayed dermal contact sensitization in the guinea pig. The test article was not considered a sensitizer in the guinea pig maximization test. | Pass | | Irritation (ISO 10993-23) | Intracutaneous Study (Polar and non-polar extraction vehicles) | The test article met the requirements of the test since the difference between each test article extract overall mean score and corresponding control extract overall mean score was 0.0 and 0.1 for the SC and SO test article extracts, respectively. | Pass | | Acute Systemic Toxicity (ISO 10993-11) | Systemic Toxicity Study (Polar and non-polar extraction vehicles) | There was no mortality or evidence of systemic toxicity from the extracts injected into mice. Each test article extract met the requirements of the study. | Pass | | Material-Mediated Pyrogenicity (USP<151>, ISO 10993-11) | Pyrogen Study - Material Mediated (Sterile non-pyrogenic saline extraction vehicle) | The total rise of rabbit temperatures during the 3 hour observation period was within acceptable USP requirements. The test article met the requirements for the absence of pyrogens. | Pass | {6}------------------------------------------------ #### COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE PREDICATE DEVICE | | Subject Device | Predicate Devices | | |-----------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------| | | EARP Nerve Cuff Electrode | Cadwell Lab | Ad-Tech Medical | | | | Disposable Stimulator Probes | Cueva Cranial Nerve Electrode | | Indications for Use | The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery. | Cadwell Disposable Stimulator Probe is used to perform localized stimulation of neural tissue and to locate, identify and monitor cranial motor nerves, peripheral nerves and spinal nerve roots during surgery. | The Cueva Cranial Nerve Electrode is intended for use to monitor cranial nerves during skull base type surgeries. | | Principle of Operation | Conducts signal between neuromonitoring equipment and nerve (interfaces w/ commercially available neuromonitoring systems) | Conducts signal between neuromonitoring equipment and nerve (interfaces w/ commercially available neuromonitoring systems) | Conducts signal between neuromonitoring equipment and nerve (interfaces w/ commercially available neuromonitoring systems) | | Product Codes /Reg# | ETN (21 CFR 874.1820) Stimulator, Nerve | ETN (21 CFR 874.1820) Stimulator, Nerve | GZL (21 CFR 882.1330) Electrode, Depth | | Duration of Use | Intraoperative (Single use) | Intraoperative (Single use) | Intraoperative (Single use) | | Implanted | No (Removed after use) | No (Removed after use) | No (Removed after use) | | Tissue Engagement | Direct nerve contact (C-shaped cuff) | Direct nerve contact (Forked tip) | Direct nerve contact (C-shaped cuff) | | Tip Contact Exposure | 2mm (Strip) | 2mm (Balls) | ~2mm (Strip) | | Electrode Exposed Surface Area | $15.4 - 42.6mm^2$ | $~25.1 - 33.2mm^2$ | $~10.4 - 14.5mm^2$ | | Bipolar or Monopolar? | Bipolar | Bipolar and monopolar versions | Monopolar | | Electrode Contact Material | Conductive metal (Platinum) | Conductive metal (Stainless Steel) | Conductive metal (Platinum) | | Electrode Insulation | Polymer (Polyimide) | Polymer (PTFE) | Polymer | | Cuff Material | Polymer (Silicone) | N/A | Polymer (Silicone) | | Lead Length | 1.8m | 2.0m | 1.8m | | Lead Wire Material | Conductive metal (Stainless steel) | Conductive metal (Tin plated copper) | Conductive metal | | Lead Wire Insulation | Polymer (FEP) | Polymer (PVC) | Polymer | | Connector Style | 1.5mm safety socket | 1.5mm safety socket | 1.5mm safety socket | | Applicator Tool Length | 260mm | 190 to 330mm (handle & shaft) | 250mm | | Provided Sterile? | Yes | Yes | Yes | #### CONCLUSION Based on testing and analysis of device characteristics, it can be concluded that the subject device does not raise new issues of safety compared to the predicate devices. The equivalent indications for use, technological characteristics, and performance characteristics for the EARP Nerve Cuff Electrode are assessed to be substantially equivalent to the predicate devices.