Who is the manufacturer of Becker External Drainage and Monitoring System?

Medtronic, Inc. filed the 510(k) submission for Becker External Drainage and Monitoring System (K200456).

What is the FDA product code for Becker External Drainage and Monitoring System?

GWM. It is classified under 21 CFR 882.1620 as a Class 2 device in the Neurology panel.

What is the regulatory pathway for Becker External Drainage and Monitoring System?

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

Who can help prepare an FDA 510(k) submission like Becker External Drainage and Monitoring System?

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.

Becker External Drainage and Monitoring System

K200456 · Medtronic, Inc. · GWM · Mar 26, 2020 · Neurology

Device Facts

Record ID	K200456
Device Name	Becker External Drainage and Monitoring System
Applicant	Medtronic, Inc.
Product Code	GWM · Neurology
Decision Date	Mar 26, 2020
Decision	SESE
Submission Type	Special
Regulation	21 CFR 882.1620
Device Class	Class 2
Attributes	Therapeutic

Indications for Use

Draining and monitoring of CSF flow from the lateral ventricles or lumbar subarachnoid space is indicated in selected patients to: 1. Reduce intracranial pressure (ICP), e.g., pre-, intra- or postoperative; 2. Monitor CSF chemistry, cytology, and physiology; 3. Provide temporary CSF drainage in patients with infected cerebrospinal fluid shunts. Monitoring of intracranial pressure (ICP) is indicated in selected patients with: 1. Severe head injury 2. Subarachnoid hemorrhage graded III, IV. or V preoperatively 3. Reyes syndrome or similar encephalopathies 4. Hydrocephalus 5. Intracranial hemorrhage 6. Miscellaneous problems when drainage is to be used as a therapeutic maneuver. Monitoring can also be used to evaluate the status pre- and postoperatively for space-occupying lesions.

Device Story

Closed system for draining/monitoring cerebrospinal fluid (CSF) from lateral ventricles or lumbar subarachnoid space; gravity-fed drainage based on system height relative to patient anatomy. Components include patient connection line, stopcocks, mounting panel, and removable 600ml drainage bag with microbial barrier vent. Used in clinical settings (e.g., ICU/neurosurgical units) by physicians/nurses. Output consists of visual CSF volume measurements and pressure monitoring via optional transducer. Facilitates therapeutic pressure reduction and diagnostic monitoring of CSF chemistry/physiology. Benefits include temporary management of intracranial pressure and drainage for infected shunts.

Clinical Evidence

No clinical data. Substantial equivalence supported by bench testing including visual/dimensional inspection, leakage testing, flow initiation pressure, seal weld integrity, and tensile strength of the inlet port.

Technological Characteristics

Sterile, single-use, non-pyrogenic system. Components: nondistensible patient line, stopcocks, mounting panel, 600ml drainage bag with hydrophobic/anti-microbial vent. Gravity-based drainage. Sterilization via Ethylene Oxide. No direct patient contact materials. Shelf life: 2 years.

Indications for Use

Indicated for patients requiring CSF drainage or ICP monitoring due to severe head injury, subarachnoid hemorrhage (grade III-V), Reyes syndrome/encephalopathies, hydrocephalus, intracranial hemorrhage, or space-occupying lesions.

Regulatory Classification

Identification

An intracranial pressure monitoring device is a device used for short-term monitoring and recording of intracranial pressures and pressure trends. The device includes the transducer, monitor, and interconnecting hardware.

Predicate Devices

Medtronic PS Medical Becker External Drainage and Monitoring System (K984053)

Submission Summary (Full Text)

{0}------------------------------------------------ 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 & Human Services logo. To the right of that is the FDA logo in blue, with the words "U.S. FOOD & DRUG" stacked on top of the word "ADMINISTRATION". March 26, 2020 Medtronic, Inc. Nancy Hampton, Ph.D. Principal Regulatory Affairs Specialist 125 Cremona Drive Goleta, California 93117 Re: K200456 Trade/Device Name: Becker External Drainage and Monitoring System Regulation Number: 21 CFR 882.1620 Regulation Name: Intracranial Pressure Monitoring Device Regulatory Class: Class II Product Code: GWM, HCA Dated: February 20, 2020 Received: February 25, 2020 # Dear Dr. Nancy Hampton: 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 {1}------------------------------------------------ 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/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 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, Xiaolin Zheng, Ph.D., M.S. Director DHT5A: Division of Neurosurgical, Neurointerventional and Neurodiagnostic Devices OHT5: Office of Neurological and Physical Medicine Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health {2}------------------------------------------------ # Indications for Use ### 510(k) Number (if known) K200456 Device Name Becker External Drainage and Monitoring System Indications for Use (Describe) Draining and monitoring of CSF flow from the lateral ventricles or lumbar subarachnoid space is indicated in selected patients to: - 1. Reduce intracranial pressure (ICP), e.g., pre-, intra- or postoperative; - 2. Monitor CSF chemistry, cytology, and physiology; - 3. Provide temporary CSF drainage in patients with infected cerebrospinal fluid shunts. Monitoring of intracranial pressure (ICP) is indicated in selected patients with: - 1. Severe head injury - 2. Subarachnoid hemorrhage graded III, IV. or V preoperatively - 3. Reyes syndrome or similar encephalopathies - 4. Hydrocephalus - 5. Intracranial hemorrhage - 6. Miscellaneous problems when drainage is to be used as a therapeutic maneuver. Monitoring can also be used to evaluate the status pre- and postoperatively for space-occupying lesions. Type of Use (Select one or both, as applicable) | Prescription Use (Part 21 CFR 801 Subpart D) | <svg height="16" width="16"> <path d="M2 2 L14 2 L14 14 L2 14 Z M3 3 L13 3 L13 13 L3 13 Z M4 4 L12 4 L12 12 L4 12 Z M5 5 L11 5 L11 11 L5 11 Z M6 6 L10 6 L10 10 L6 10 Z M7 7 L9 7 L9 9 L7 9 Z" fill="black"></path> <path d="M4 4 L12 12 M12 4 L4 12" stroke="black" stroke-width="2"></path> </svg> | |------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Over-The-Counter Use (21 CFR 801 Subpart C) | <svg height="16" width="16"> <path d="M2 2 L14 2 L14 14 L2 14 Z M3 3 L13 3 L13 13 L3 13 Z M4 4 L12 4 L12 12 L4 12 Z M5 5 L11 5 L11 11 L5 11 Z M6 6 L10 6 L10 10 L6 10 Z M7 7 L9 7 L9 9 L7 9 Z" fill="white"></path> </svg> | ### 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." {3}------------------------------------------------ ### Becker® External Drainage and Monitoring System 510(k) Summary March 26, 2020 - I. Medtronic, Inc. Company: Medtronic Neurosurgery 125 Cremona Drive Goleta, California 93117 USA - Contact: Nancy Hampton, PhD Principal Regulatory Affairs Specialist nancy.d.hampton@medtronic.com Telephone Number: 949-490-3773 - Establishment Registration Number: 2021898 II. - III. Proprietary Trade Name: Becker® External Drainage and Monitoring System - IV. Regulatory Class: II #### V. Primary Classification: Name: Intracranial pressure monitoring device. Product Code: GWM Regulation: 21 CFR 882.1620 ## Secondary Classification: Name: Ventricular catheter Product Code: HCA Regulation:21 CFR 882.4100 #### VI. Product Description: The Becker External Drainage and Monitoring System (Becker EDMS) provides the physician with a complete closed system for: 1. Draining cerebrospinal fluid (CSF) from the lateral ventricles of the brain or the lumbar subarachnoid space. {4}------------------------------------------------ 2. Monitoring CSF pressure and flow rate from the lateral ventricles of the brain and the lumbar subarachnoid space. The Becker EDMS consists of a nondistensible blue or green striped (proximal end) patient connection line, patient line stopcock, mounting panel/main system section, two latex-free injection sites and a removable drainage bag with approximate volumetric graduations and microbial barrier air vent. The main system section located on the mounting panel includes: - 1. Mounting bracket for height adjustment of system - Optional self-adjusting cord with lock for adjustment of system height 2. - 3. Main system stopcock with optional transducer attachment location - Sliding, graduated, 50 cc drip chamber with drip former and conical bottom, and locking 4. bracket - 5. Two drainage line slide clamps for flow monitoring and sampling - Drainage bag connection line 6. - Needleless Injection Site (Interlink or Smartsite) 7. - Instructions for Use 8. The system does not contain any latex components. #### VII. Indications for Use: Draining and monitoring of CSF flow from the lateral ventricles or lumbar subarachnoid space is indicated in selected patients to: - 1. Reduce intracranial pressure (ICP), e.g., pre-, intra- or postoperative; - 2. Monitor CSF chemistry, cytology, and physiology; - 3. Provide temporary CSF drainage in patients with infected cerebrospinal fluid shunts. Monitoring of intracranial pressure (ICP) is indicated in selected patients with: - 1. Severe head injury - 2. Subarachnoid hemorrhage graded III, IV, or V preoperatively - 3. Reyes syndrome or similar encephalopathies - 4. Hydrocephalus - 5. Intracranial hemorrhage - 6. Miscellaneous problems when drainage is to be used as a therapeutic maneuver. Monitoring can also be used to evaluate the status pre- and postoperatively for space-occupying lesions. #### VIII. Summary of the Technological Characteristics: The proposed Becker EDMS modified disposable bag is a sterile nonpyrogenic single use component of the system that is removable from the Becker EDMS mounting panel. The bag has an approximate volume capacity of 600ml with approximate volumetric markings in 50mL increments, an inlet port, an outlet port and a hydrophobic/anti-microbial vent embedded into the body of the bag. The rest of the Becker EDMS system has the same technological characteristics as the predicate device. {5}------------------------------------------------ | | Subject Device | Predicate Device | |------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | | K984053 | | Intended use / Indications for Use | Draining and monitoring of CSF flow from the lateral ventricles or lumbar subarachnoid space is indicated in selected patients to: 1. Reduce intracranial pressure (ICP), e.g., pre-, intra- or postoperative; 2. Monitor CSF chemistry, cytology, and physiology; 3. Provide temporary CSF drainage in patients with infected cerebrospinal fluid shunts. Monitoring of intracranial pressure (ICP) is indicated in selected patients with: 1. Severe head injury 2. Subarachnoid hemorrhage graded III, IV, or V preoperatively 3. Reyes syndrome or similar encephalopathies 4. Hydrocephalus 5. Intracranial hemorrhage 6. Miscellaneous problems when drainage is to be used as a therapeutic maneuver. Monitoring can also be used to evaluate the status pre- and postoperatively for space-occupying lesions. | Draining and monitoring of CSF flow from the lateral ventricles or lumbar subarachnoid space is indicated in selected patients to reduce intracranial pressure (ICP), e.g. pre- intra- or postoperative; monitor CSF chemistry, cytology and physiology; provide temporary CSF drainage in patients with infected cerebrospinal fluid shunts. The monitoring of the intracranial pressure (ICP) is indicated in selected patients with severe head injury; subarachnoid hemorrhage graded III, IV or V preoperatively; Reyes syndrome or similar encephalopathies; hydrocephalus; intracranial hemorrhage or miscellaneous problems when drainage is to be used as a therapeutic maneuver. Monitoring can also be used to evaluate the status pre-and postoperatively for space occupying lesions. | | Operating Principle | External drainage is temporary drainage of cerebrospinal fluid (CSF) from the lateral ventricles of the brain, or the lumbar space of the spine, into an external collection bag. The Becker EDMS drains CSF by using a combination of gravity and intercerebral pressure. The drainage rate depends on the height at which the system is placed relative to the patient's anatomy. | Same | | Materials | There are no materials with direct patient contact | Same | | Anatomical Sites | Drainage and monitoring of CSF flow from the lateral ventricles or lumbar subarachnoid space. | Same | | Biocompatibility | No direct patient contact. In contact with CSF | Same | | | Subject Device | Predicate Device K984053 | | Sterilization Method | Ethylene Oxide | Same | | Pyrogenicity | Non pyrogenic | Same | | Shelf life | 2 years | Same | {6}------------------------------------------------ - IX. Identification of Legally Marketing Predicate Devices: Medtronic PS Medical Becker External Drainage and Monitoring System, K984053. #### X. Discussion of the Performance Testing: In accordance with the risk assessment of the change it was determined that dimensional verification, and design verification testing of the bag was necessary. The successful results of the testing demonstrated that the changes do not raise questions of safety and effectiveness, supporting the substantial equivalence to the predicate device. | Test | Test Method Summary / Purpose | Results | |---------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------| | Visual and Dimensional Inspection | Visual and dimensional inspection demonstrates that the printed graduations meet volumetric capacity. Volumetric graduations are approximate. | The Becker EDMS device met the acceptance criteria for visual and dimensional inspection. | | Leakage of Drainage Bag | The drainage bag must withstand being inverted without leaking. | The Becker EDMS device met the acceptance criteria for drainage bag leakage. | | Flow Initiation Pressure | Record pressure at which flow initiates, for each drainage bag. | The Becker EDMS device met the acceptance criteria for flow initiation pressure. | | Drainage Bag Seal Weld | Ensure there are no leaks in the drainage bag. | The Becker EDMS device met the acceptance criteria for drainage bag seal weld. | | Tensile Strength of Drainage Bag Inlet Port | Evaluate the tensile strength of the drainage bag inlet port to failure. | The Becker EDMS device met the acceptance criteria for tensile strength of drainage bag inlet port. | ## Performance Data - Bench # Performance Data – Animal The risk assessment of the proposed modifications to the disposable bag did not require animal testing. Determination of substantial equivalence for the design change is based upon the design verification bench testing. {7}------------------------------------------------ ## Performance Data – Clinical The risk assessment of the proposed modifications to the disposable bag did not require clinical testing. Determination of substantial equivalence for the design change is based upon the design verification bench testing. #### XI. Conclusions: The information provided in this submission demonstrates that the subject device Becker EDMS has the same intended use/indications for use as the predicate device and the differences in technological characteristics introduced by the proposed changes to the disposable bag do not raise questions of safety and effectiveness. Based on the information provided in this submission the subject Becker EDMS device is considered substantially equivalent to the previously cleared predicate device.

Becker External Drainage and Monitoring System

Device Facts

Indications for Use

Device Story

Clinical Evidence

Technological Characteristics

Indications for Use

Regulatory Classification

Identification

Predicate Devices

Submission Summary (Full Text)

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Becker External Drainage and Monitoring System

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Indications for Use

Device Story

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Submission Summary (Full Text)

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